HOW TO STEP BY STEP DEMONSTRATE MOTOR EXAMINATION IN NEUROLOGY ASSESSMENT IN DEATIL

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Motor Examination in Neurological Assessment — Step-by-Step Guide

The motor examination is a systematic evaluation of the motor system, covering inspection, tone, power, reflexes, coordination, and gait. Each component localizes lesions to specific parts of the neuraxis.

PREPARATION

  • Position the patient comfortably, ideally supine or seated
  • Expose the limbs adequately for inspection
  • Explain each step to gain cooperation
  • Compare right vs. left and upper vs. lower limbs throughout

STEP 1 — INSPECTION (Look Before You Touch)

Observe the patient at rest before any active testing:
What to Look ForSignificance
Muscle wasting/atrophyLower motor neuron (LMN) lesion, disuse, myopathy
Fasciculations (spontaneous twitching)LMN disease (e.g., motor neurone disease)
TremorResting tremor → Parkinson's; intention tremor → cerebellar
Dystonia / chorea / myoclonusExtrapyramidal or cortical pathology
Posture of limbsHemiplegia: flexed arm, extended leg; LP: pronator drift
Scars / deformitiesPrior injury, surgery, congenital causes

STEP 2 — MUSCLE TONE

Technique:
  1. Ask the patient to fully relax — "Let your arm go completely floppy."
  2. Support the limb and passively move each joint through full range in an unpredictable rhythm (vary speed and direction to avoid voluntary cooperation).
Upper limb: Pronate/supinate the wrist; flex/extend the elbow Lower limb: Roll the leg at the hip; flex/extend the knee; dorsiflex the ankle
FindingDescriptionCause
NormalSlight resistance throughout range
Spasticity"Clasp-knife" — increased resistance then sudden give; velocity-dependentUMN lesion (corticospinal tract)
RigidityConstant resistance throughout range ("lead pipe")Extrapyramidal lesion
Cogwheel rigidityRigidity + superimposed ratchet-like catchesParkinson's disease
Flaccidity / hypotoniaNo resistance; limb feels floppyLMN lesion, cerebellar disease, acute UMN shock
Tip: To unmask subtle cogwheeling, ask the patient to move the other hand while you passively move the tested wrist.

STEP 3 — MUSCLE POWER (MRC Scale)

Test each muscle group individually, starting proximally and moving distally. Stabilize the proximal joint, then ask the patient to move against resistance.

MRC Power Grading Scale

(from Textbook of Family Medicine, 9e)
GradeDescription
5Normal — full power against full resistance
4Weak but can overcome gravity plus some resistance
3Can move against gravity but not additional resistance
2Movement possible but cannot overcome gravity (test in horizontal plane)
1Visible/palpable muscle contraction, no joint movement
0No contraction at all

Upper Limb Muscles to Test

MovementNerve RootNerve
Shoulder abductionC5Axillary
Elbow flexionC5–C6Musculocutaneous
Elbow extensionC7Radial
Wrist extensionC6–C7Radial
Finger extensionC7Posterior interosseous
Finger flexionC8Median/ulnar
Finger abduction (interossei)T1Ulnar
Thumb oppositionT1Median

Lower Limb Muscles to Test

MovementNerve RootNerve
Hip flexionL1–L2Femoral
Hip extensionS1Inferior gluteal
Knee extensionL3–L4Femoral
Knee flexionS1Sciatic
Ankle dorsiflexionL4–L5Common peroneal
Ankle plantarflexionS1–S2Tibial
Great toe extensionL5Deep peroneal
Pronator drift test: Ask the patient to hold both arms outstretched, palms up, eyes closed. A pyramidal (UMN) lesion causes the arm to pronate and drift downward on the affected side.
Manual muscle testing technique
Manual muscle testing of the foot — MRC grading technique
Hand nerve motor examination

STEP 4 — DEEP TENDON REFLEXES (DTRs)

Use a tendon hammer to strike the tendon briskly. The patient must be relaxed. If a reflex is absent, use reinforcement (Jendrassik manoeuvre: patient interlocks fingers and pulls apart while you test the lower limb).

Reflex Grading Scale

GradeResponse
0Absent
1+Diminished
2+Normal
3+Brisk (possibly pathological)
4+Clonus — pathological

Reflexes and Their Root Levels

(from Textbook of Family Medicine, 9e, Table 41-1)
ReflexRootTechnique
BicepsC5Place your thumb on the biceps tendon; strike your thumb
Supinator (brachioradialis)C6Strike the radial border of the wrist, 4 cm above the wrist
TricepsC7Strike the triceps tendon above the olecranon, elbow at 90°
FingerC8Place your fingers across the patient's partially flexed fingers; strike
Knee (patellar)L3–L4Legs hanging free or supported; strike patellar tendon
Ankle (Achilles)S1–S2Dorsiflex foot slightly; strike Achilles tendon
Patellar tendon reflex with Jendrassik manoeuvre
Patellar reflex elicitation with Jendrassik reinforcement manoeuvre — L3/L4 testing
Achilles tendon reflex technique
Achilles tendon reflex — kneeling position technique, S1/S2

STEP 5 — PLANTAR RESPONSE (Babinski Sign)

Technique:
  1. Use a blunt object (key or stick end of reflex hammer)
  2. Stroke firmly from the lateral heel along the lateral sole, then curve medially under the metatarsal heads
  3. Observe the big toe response
ResponseNameSignificance
Toe flexion (curls down)Flexor responseNormal in adults
Big toe extension + fan out of other toesBabinski positive (extensor)UMN lesion — corticospinal tract damage
Babinski sign elicitation technique
Babinski sign — lateral sole stroking technique

STEP 6 — COORDINATION

Tests the cerebellar system. The patient must have adequate power to perform these tests meaningfully.

Upper Limb

Finger-to-Nose Test:
  1. Ask the patient to fully extend the arm
  2. Touch the tip of their nose, then touch the examiner's index finger (held at arm's length)
  3. Repeat after the examiner moves the target finger to a new location
Dysdiadochokinesia:
  • Ask the patient to perform rapid alternating hand movements (pronate/supinate rapidly on the other palm)
  • Cerebellar lesion → irregular, slow, clumsy
Finger tapping: Tap index finger to thumb rapidly; assess speed, regularity, and symmetry

Lower Limb

Heel-Knee-Shin Test:
  1. Patient lies supine
  2. Place heel on the opposite knee
  3. Slide the heel smoothly down the shin to the ankle
  4. Repeat; assess smoothness and accuracy
FindingSignificance
Dysmetria — past-pointing, overshootingCerebellar lesion (ipsilateral hemisphere)
Intention tremor — worsens as approaching targetCerebellar
Decomposition of movementCerebellar
Finger-to-nose test
Finger-to-nose test for cerebellar coordination assessment

STEP 7 — GAIT ASSESSMENT

Always examine gait — it integrates the entire motor system in one observation.
Gait PatternDescriptionCause
HemiplegicOne arm flexed, leg circumducts (swings out in arc)Unilateral UMN (cortical/capsular)
Spastic ("scissor")Both legs stiff, cross over ("scissors")Bilateral UMN
SteppageHigh steppage, foot slaps down, cannot dorsiflexFootdrop (L4/L5 or peroneal nerve)
WaddlingTrunk sways side-to-sideProximal muscle weakness (myopathy, muscular dystrophy)
ParkinsonianStooped, shuffling small steps, reduced arm swing, festinationExtrapyramidal
Cerebellar (ataxic)Wide-based, unsteady, irregular, unable to tandem walkCerebellar pathology
Sensory ataxicStamping gait, worsens eyes closedProprioceptive loss (posterior columns)
Additional gait tests:
  • Tandem walking (heel-to-toe in a straight line) — uncovers subtle cerebellar ataxia
  • Walking on heels — tests L4/L5 (tibialis anterior)
  • Walking on tiptoes — tests S1 (gastrocnemius)
  • Romberg test: Stand feet together; positive if patient falls/sways markedly with eyes closed → dorsal column or peripheral proprioceptive loss

STEP 8 — INTEGRATION: UMN vs. LMN Localisation

FeatureUMN LesionLMN Lesion
ToneIncreased (spasticity)Decreased (flaccidity)
PowerReduced (pyramidal pattern)Reduced (wasted distribution)
ReflexesHyperreflexia (3–4+)Hyporeflexia / absent (0–1+)
BabinskiExtensor (positive)Flexor (normal) or absent
WastingMild (disuse)Prominent / severe
FasciculationsAbsentPresent
ClonusMay be presentAbsent

CLINICAL PEARL: Functional Weakness

A patient with functional (non-organic) weakness has:
  • Normal tone
  • Normal reflexes
  • No wasting
  • Erratic, variable power (give-way weakness)
Use Hoover's sign: ask the patient to lift the weak leg — normally the other heel presses down involuntarily; in functional weakness this involuntary movement is absent.

Sources: Textbook of Family Medicine, 9e — Motor Examination; Plum and Posner's Diagnosis and Treatment of Stupor and Coma

IN DETAIL EACH ONE LIKE INSPECTION EACH STEP PROPERLY

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Now I have all the detail needed from Harrison's (22e) and Adams & Victor's. Let me compose the full, exhaustive step-by-step guide.

MOTOR EXAMINATION IN NEUROLOGY — COMPLETE STEP-BY-STEP DETAIL


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STEP 1 — INSPECTION (LOOK BEFORE YOU TOUCH)

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Inspection is the most undervalued component. It costs nothing and reveals everything — a skilled examiner can localise a lesion before touching the patient.

1A. PREPARATION FOR INSPECTION

Before you begin:
  • Ensure the room is well-lit — fasciculations are invisible in dim light
  • Ask the patient to undress to underwear so all four limbs and trunk are visible
  • Position the patient comfortably supine initially, then seated
  • Stand back at least 1–2 metres for a panoramic view first
  • Tell the patient: "I am going to look at your muscles before I test them. Please stay relaxed."

1B. INSPECT THE WHOLE BODY POSTURE FIRST

Look at the patient's resting posture from the foot of the bed:
What You SeeWhat It Means
One arm flexed at elbow and wrist, leg extended and internally rotatedEstablished UMN (cortical or capsular) hemiplegia — posture of spasticity
Both legs extended and stiff, arms drawn inBilateral UMN — paraplegia or quadriplegia
Limb lying externally rotated and floppyLMN lesion or acute UMN (flaccid phase)
Flexed, stooped posture at restParkinson's disease / extrapyramidal disorder
Head tilted, asymmetric shoulder heightTorticollis, scoliosis, muscle imbalance

1C. INSPECT FOR MUSCLE WASTING (ATROPHY)

Work systematically: proximal → distal, both sides.
Technique:
  1. Compare the same muscle group on both sides simultaneously
  2. Look for hollowing, loss of normal contour, prominent bony landmarks
Specific areas to examine:
Body PartWhat to Look ForHow to Identify
Thenar eminence (thumb base)Flattening — median nerve or C8/T1Compare thumb base bulk bilaterally
Hypothenar eminence (little finger)Wasting — ulnar nerve or C8/T1Look at medial palm contour
Dorsal interosseiGuttering between metacarpalsAsk patient to fan fingers; look at dorsal hand
Forearm musclesAsymmetric bulkCompare circumference of both forearms
Biceps/tricepsHollowing of upper armCompare upper arm contour
DeltoidFlat, square shoulder contourCompare shoulder fullness
Supraspinatus/infraspinatusHollowing above/below spine of scapulaView from behind
QuadricepsHollowing above patellaCompare thighs with legs straight
Calf (gastrocnemius)Loss of normal rounded calf bulkCompare both calves
Small muscles of footIntrinsic wastingLook at dorsum of foot; arching
TongueAtrophy, wrinkled surfaceAsk patient to open mouth — inspect at rest
Temporalis/masseterTemporal hollowing, flat cheekLook at face in good light
Grading wasting: Document as mild, moderate, or severe. Note whether it is focal (single nerve or root), distal (peripheral neuropathy), proximal (myopathy), or hemibody (UMN).
Significance:
  • Significant wasting = LMN lesion (nerve, root, anterior horn cell) or primary muscle disease
  • UMN lesions produce only mild disuse atrophy over months — never the severe hollowing of a LMN lesion
Bilateral lower limb muscle wasting — LMN pattern
Severe bilateral lower limb muscle wasting with prominent bony landmarks — chronic LMN / denervation pattern
Asymmetric shoulder girdle wasting
Left shoulder girdle wasting with loss of deltoid, supraspinatus, infraspinatus — LMN/plexus lesion

1D. INSPECT FOR FASCICULATIONS

What they are: Spontaneous, random, brief twitches of a motor unit visible under the skin — caused by denervation hypersensitivity of anterior horn cells or motor axons.
How to observe:
  1. The patient must be completely at rest and the room must be well-lit (tangential lighting helps)
  2. Watch each muscle group for at least 15–30 seconds before moving on
  3. Ask the patient not to contract the muscle — fasciculations appear at rest
  4. Gently tapping a muscle may provoke fasciculations if denervation is present
Where to look specifically:
  • Tongue (ask patient to rest tongue on floor of mouth — do NOT protrude, as movement mimics fasciculations)
  • Thenar/hypothenar eminences
  • Deltoid
  • Quadriceps (large, easy to see)
  • Calf
FindingSignificance
Fasciculations alone (no weakness, no wasting)Benign fasciculation syndrome — very common
Fasciculations + wasting + weaknessLMN pathology — motor neurone disease (ALS), radiculopathy, peripheral neuropathy
Tongue fasciculationsBulbar LMN involvement — ALS, progressive bulbar palsy
Key rule: Fasciculations are never seen in pure UMN lesions.

1E. INSPECT FOR INVOLUNTARY MOVEMENTS

Observe with the patient at rest, maintaining a posture, and during voluntary movement.
Involuntary MovementWhen It OccursDescriptionCause
Resting tremorAt rest, disappears with movementPill-rolling, 4–6 Hz, one handParkinson's disease
Postural/action tremorWhen holding posture (arms outstretched)Fine, 8–12 HzEssential tremor, physiological, thyrotoxicosis
Intention tremorDuring voluntary movement, worsens near targetCoarse, oscillatingCerebellar lesion (ipsilateral)
ChoreaContinuous, random, flowingBrief, irregular, dance-like limb jerksHuntington's, Sydenham's, drugs
AthetosisSlow, writhingContinuous, sinuous twisting of distal limbsBasal ganglia lesion
HemiballismusSudden, flingingViolent, high-amplitude proximal flingingContralateral subthalamic nucleus lesion
MyoclonusBrief shock-like jerksAt rest or with movementCortical, subcortical, spinal causes
TicsSuppressible, stereotypedRepetitive semi-purposeful movementsTourette's syndrome, habit
DystoniaSustained twisting postureProlonged abnormal postureFocal or generalised dystonia

1F. INSPECT THE SKIN, JOINTS, AND DEFORMITIES

What to Look ForSignificance
Scars / surgery scarsNerve trauma, previous decompression
Pressure sores / callusesChronic immobility, loss of sensation
Joint deformities / contracturesChronic spasticity, disuse
Pes cavus (high arch)Hereditary motor/sensory neuropathy (Charcot-Marie-Tooth)
Hammer toesLong-standing intrinsic wasting
Café-au-lait spots / neurofibromasNeurofibromatosis
Skin rash over knuckles (Gottron's papules)Dermatomyositis


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STEP 2 — MUSCLE TONE

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2A. PRINCIPLES

  • Tone = the resistance of a muscle to passive stretch at rest
  • It reflects the integrity of the reflex arc + supraspinal control
  • The patient must be completely relaxed — actively distract them during testing
  • Move joints at varying speeds and in unpredictable directions to prevent voluntary assistance

2B. UPPER LIMB TONE — STEP BY STEP

Step 1 — Wrist pronation/supination:
  1. Support the patient's forearm with one hand
  2. Hold the patient's hand with your other hand as if shaking hands
  3. Pronate and supinate the wrist repeatedly at varying speeds
  4. Feel for resistance throughout the range
Step 2 — Wrist flexion/extension:
  1. Cup the patient's hand
  2. Flex and extend the wrist passively, varying speed
  3. Normal: slight springy resistance throughout
Step 3 — Elbow flexion/extension:
  1. Support the forearm and flex/extend the elbow
  2. Do this at different speeds — spasticity is velocity-dependent
Step 4 — Shoulder movement:
  1. Hold the upper arm and gently internally/externally rotate and abduct
  2. Useful for detecting shoulder rigidity in Parkinson's

2C. LOWER LIMB TONE — STEP BY STEP

Step 1 — Leg roll test:
  1. Patient lies supine, legs extended
  2. Place both hands on the thigh and briskly roll the leg internally and externally
  3. Watch the foot — it should oscillate freely
  4. In spasticity, the foot does not oscillate freely and moves rigidly with the leg
Step 2 — Knee lift test (Harrison's method):
  1. Place both hands behind the patient's knee
  2. Rapidly lift the knee off the table
  3. Observe the heel:
    • Normal: heel drags along the table surface for a variable distance before lifting
    • Increased tone (spasticity): heel lifts immediately with the knee — no drag
    • Decreased tone (flaccidity): heel stays on the table even as you lift fully
Step 3 — Ankle tone / clonus:
  1. With the knee slightly flexed, place your hand under the ankle
  2. Dorsiflex the foot rapidly and sustain the stretch
  3. Sustained rhythmic beats = clonus — indicates UMN lesion (corticospinal tract damage)
  4. Count the beats — more than 5 sustained beats = pathological clonus
Step 4 — Patellar clonus:
  1. Patient lies flat with leg extended
  2. Push the patella sharply downward and hold
  3. Rhythmic patellar oscillation = patellar clonus — UMN sign

2D. TYPES OF ABNORMAL TONE — DETAILED

TypeFeelDistributionVelocity-DependentCause
SpasticityInitial resistance then sudden "give" (clasp-knife)Flexors (UL), Extensors (LL)Yes — worse with fast movementCorticospinal tract lesion
Lead-pipe rigidityConstant, uniform resistance in all directions throughout rangeFlexors = ExtensorsNoExtrapyramidal (Parkinson's)
Cogwheel rigidityRatchet-like interruptions superimposed on rigidityAs aboveNoParkinson's (rigidity + tremor)
Paratonia (Gegenhalten)Variable, unpredictable — patient seems to resist your movements despite instructionAny distributionIrregularFrontal lobe disease, dementia
Flaccidity / hypotoniaNo resistance; limb feels heavy, floppyDiffuse or segmentalN/ALMN, peripheral nerve, cerebellar, acute UMN (spinal shock)
To bring out cogwheel rigidity: Ask the patient to move the opposite hand (e.g., open and close it) while you assess the tested wrist — this "reinforcement" makes subtle cogwheeling much more apparent. — Harrison's Principles of Internal Medicine, 22e
Modified Ashworth Scale assessment — passive elbow movement for tone
Passive elbow movement to assess spasticity using Modified Ashworth Scale methodology


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STEP 3 — MUSCLE POWER (STRENGTH)

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3A. PRINCIPLES

  • Always isolate the muscle being tested — stabilise the proximal joint
  • Apply resistance in the direction opposing the movement
  • Ask for maximum effort: "Push as hard as you can — don't let me move you"
  • Palpate the contracting muscle while testing — confirms effort and contraction quality
  • Compare left vs. right at each level
  • Grade using the MRC Scale

3B. MRC POWER GRADING — DETAILED

(Harrison's Principles of Internal Medicine, 22e)
GradeClinical MeaningPractical Test
5Full power — normalResists maximal examiner effort
4+Movement against strong resistanceSlightly less than normal
4Movement against moderate resistanceSome weakness but functional
4−Movement against mild resistanceNoticeably weak
3Movement against gravity but not against any resistanceCan lift limb fully off table
2Movement with gravity eliminated (horizontal plane)Cannot lift against gravity; test lying flat
1Flicker or trace of contraction — no joint movementBarely palpable contraction
0No contraction whatsoeverNothing palpable

3C. PRONATOR DRIFT TEST — SCREEN FOR UMN WEAKNESS

This is the single most useful screening test for upper limb pyramidal weakness.
How to perform:
  1. Ask the patient to hold both arms fully outstretched, palms facing upward (supinated), parallel to the floor
  2. Ask them to close their eyes
  3. Hold this position for 10 seconds
  4. Watch carefully for any:
    • Pronation of the forearm (palm turns down)
    • Downward drift of the entire arm
    • Finger flexion
What you see:
FindingSignificance
Pronation + downward drift, asymmetricPyramidal (UMN) weakness on that side
Upward driftProprioceptive or sensory loss (posterior column)
Bilateral symmetrical driftFunctional / non-organic, or cerebellar
No driftScreen is negative for pyramidal weakness
"Testing for pronator drift is an extremely useful method for screening upper limb weakness." — Harrison's, 22e

3D. UPPER LIMB POWER — STEP-BY-STEP MUSCLE TESTING

Test in this order: proximal → distal

Shoulder Abduction (C5, Axillary nerve)

  • Position: Patient seated, arm at 90° abduction
  • Your hand: Place on the lateral upper arm
  • Command: "Hold your arm up — don't let me push it down"
  • Resistance: Push the arm downward toward the side

Shoulder Adduction (C6–C7, Pectoral nerve)

  • Position: Arm at 90° abduction
  • Command: "Push your arm into your side — don't let me pull it out"
  • Resistance: Pull the arm outward

Elbow Flexion (C5–C6, Musculocutaneous nerve — Biceps)

  • Position: Elbow at 90°, forearm supinated
  • Your hand: Grasp the wrist
  • Command: "Bend your elbow — don't let me straighten it"
  • Resistance: Pull the forearm downward (extending the elbow)

Elbow Extension (C7, Radial nerve — Triceps)

  • Position: Elbow at 90°, forearm pronated
  • Command: "Straighten your arm — don't let me bend it"
  • Resistance: Push the forearm upward (flexing the elbow)

Wrist Extension (C6–C7, Radial nerve)

  • Position: Forearm pronated, fist loosely closed
  • Command: "Cock your wrist back — don't let me push it forward"
  • Resistance: Push the dorsum of the hand into flexion

Wrist Flexion (C7–C8, Median/Ulnar nerve)

  • Command: "Flex your wrist — don't let me pull it back"
  • Resistance: Push the palm into extension

Finger Extension (C7, Posterior interosseous nerve)

  • Position: Fingers extended at MCP joints
  • Command: "Keep your fingers straight — don't let me bend them"
  • Resistance: Push fingers into flexion at MCP joints

Finger Flexion (C8, Median/Ulnar nerve)

  • Command: "Squeeze my fingers as hard as you can"
  • Insert two fingers into the patient's fist — assess grip strength

Finger Abduction / Interossei (T1, Ulnar nerve)

  • Position: Hand flat on a surface, fingers extended
  • Command: "Spread your fingers apart — don't let me push them together"
  • Resistance: Push middle and index finger together

Thumb Opposition (T1, Median nerve — Thenar muscles)

  • Command: "Touch your little finger with your thumb — keep them together"
  • Try to pull the thumb away from the little finger

3E. LOWER LIMB POWER — STEP-BY-STEP MUSCLE TESTING

Hip Flexion (L1–L2, Femoral nerve — Iliopsoas)

  • Position: Patient supine, hip flexed to 30°
  • Command: "Lift your leg off the bed — don't let me push it down"
  • Resistance: Push the thigh downward

Hip Extension (S1, Inferior gluteal nerve — Gluteus maximus)

  • Position: Patient supine, leg flat
  • Command: "Push your heel down into the bed — don't let me lift your leg"
  • Or: prone — "Lift your straight leg off the bed"

Hip Abduction (L4–L5, Superior gluteal nerve — Gluteus medius)

  • Position: Supine, legs flat
  • Command: "Push your leg out to the side — don't let me push it in"
  • Resistance: Push the lateral thigh inward

Hip Adduction (L2–L3, Obturator nerve)

  • Command: "Squeeze your legs together — don't let me pull them apart"

Knee Extension (L3–L4, Femoral nerve — Quadriceps)

  • Position: Seated or supine with knee at 90°
  • Command: "Straighten your knee — don't let me bend it"
  • Resistance: Push the lower leg into flexion

Knee Flexion (S1, Sciatic nerve — Hamstrings)

  • Position: Prone or supine with knee slightly flexed
  • Command: "Bend your knee — don't let me straighten it"
  • Resistance: Pull the lower leg into extension

Ankle Dorsiflexion (L4–L5, Deep peroneal nerve — Tibialis anterior)

  • Command: "Pull your foot up toward you — don't let me push it down"
  • Resistance: Push down on the dorsum of the foot
  • Weakness = footdrop, steppage gait

Ankle Plantarflexion (S1–S2, Tibial nerve — Gastrocnemius/Soleus)

  • Command: "Push your foot down like pressing a pedal — don't let me pull it up"
  • Resistance: Push upward on the sole
  • Also test: can the patient stand on tiptoe on each foot in turn?

Great Toe Extension (L5, Deep peroneal nerve — Extensor hallucis longus)

  • Command: "Pull your big toe up — don't let me push it down"
  • Resistance: Push the big toe into plantarflexion

3F. RECOGNISING WEAKNESS PATTERNS

PatternDescriptionLocalisation
Pyramidal / UMN patternUpper limb: extensors weak > flexors. Lower limb: flexors weak > extensorsCorticospinal tract (cortex, capsule, cord)
Proximal > distal weaknessDifficulty rising from chair, lifting arms overheadMyopathy, muscular dystrophy
Distal > proximal weaknessWrist/finger drop, footdropPeripheral neuropathy
Single nerve distributionFollows anatomical territory of one nerve exactlyMononeuropathy
Dermatomal / myotomalFollows a nerve root distributionRadiculopathy
Bulbar weaknessFacial, tongue, palatal, swallowingMotor neurone disease, brainstem


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STEP 4 — DEEP TENDON REFLEXES (DTRs)

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4A. PRINCIPLES

  • The patient must be relaxed — contracted muscles abolish reflexes
  • Use a proper tendon hammer (Babinski or Queen Square hammer)
  • Strike the tendon (not the muscle belly) with a brisk, relaxed wrist flick
  • Assess the smallest stimulus needed to elicit the reflex, not the maximum response
  • Always compare left vs. right at each level
  • If absent, use Jendrassik manoeuvre before concluding the reflex is truly absent

4B. JENDRASSIK MANOEUVRE (Reinforcement)

For lower limbs:
  • Ask the patient to interlock their fingers of both hands and pull them apart vigorously
  • While they are pulling — strike the tendon
  • This reduces cortical inhibition and unmasks suppressed reflexes
For upper limbs:
  • Ask the patient to clench their teeth or clench the opposite fist

4C. REFLEX GRADING SCALE

(Harrison's Principles of Internal Medicine, 22e)
GradeDescription
0Absent — even with reinforcement
1+Present but diminished
2+Normal
3+Brisk — possibly pathological (assess in context)
4+Clonus — definitely pathological

4D. UPPER LIMB REFLEXES — HOW TO ELICIT EACH

Biceps Reflex (C5, C6)

  1. Patient's arm relaxed, elbow at 90° flexion, forearm slightly pronated (resting on your arm)
  2. Place your thumb firmly over the biceps tendon (in the antecubital fossa)
  3. Strike your thumb with the hammer — not the patient directly
  4. Normal response: Biceps contracts → elbow flexion + slight supination
  5. Absent: C5/C6 lesion
  6. Exaggerated: UMN lesion above C5

Supinator (Brachioradialis) Reflex (C5, C6)

  1. Patient's arm relaxed, elbow at 90°, forearm in mid-pronation (thumb up)
  2. Strike the radial border of the forearm 4–5 cm above the wrist
  3. Normal response: Forearm flexion + slight supination
  4. Inverted supinator reflex: No contraction here but fingers flex → C5/C6 root lesion with intact C8 reflex arc — significant for cord lesion at C5/C6

Triceps Reflex (C6, C7)

  1. Support the patient's arm with elbow at 90° flexion, arm hanging freely
  2. Strike the triceps tendon directly above the olecranon
  3. Normal response: Elbow extension
  4. Absent: C7 lesion

Finger Flexor Reflex (C8, T1)

  1. Hold the patient's hand with their fingers slightly flexed over your fingers
  2. Strike the dorsal surface of your fingers
  3. Normal: Slight finger flexion
  4. Exaggerated: Pathological — Hoffmann's sign equivalent; UMN
  5. Hoffmann's sign: Flick the middle fingernail downward and release — thumb and index finger flex involuntarily = UMN sign

4E. LOWER LIMB REFLEXES — HOW TO ELICIT EACH

Knee (Patellar) Reflex (L3, L4)

Method 1 — Seated:
  1. Patient sits with legs hanging freely at 90° off the bed edge
  2. Strike the patellar tendon just below the patella with a brisk swing
  3. Normal: Knee extension (quadriceps contraction)
Method 2 — Supine:
  1. Support the knee with your non-dominant arm underneath, creating a 30° knee flex
  2. Strike the patellar tendon
  3. Watch for quadriceps contraction and knee extension
Patellar reflex with Jendrassik reinforcement
Patellar reflex with Jendrassik reinforcement — knee at 90°, feet clear of floor

Ankle (Achilles) Reflex (S1, S2)

Method 1 — Kneeling position (preferred):
  1. Ask the patient to kneel on the examination couch with feet hanging over the edge
  2. Slightly dorsiflex the foot to put the tendon under mild tension
  3. Strike the Achilles tendon directly, above the heel
Method 2 — Supine, figure-4:
  1. Cross the tested leg over the opposite shin ("figure-4")
  2. Gently dorsiflex the foot
  3. Strike the Achilles tendon
Method 3 — Supine, knee supported:
  1. Flex the hip and knee, let the leg fall laterally
  2. Apply passive dorsiflexion, then strike
Normal: Plantarflexion of the foot
Achilles reflex — figure-4 position
Achilles reflex in figure-4 position with passive dorsiflexion — S1/S2

4F. CUTANEOUS (SUPERFICIAL) REFLEXES

Plantar Reflex / Babinski Sign

  1. Position the patient's leg in external rotation, knee slightly flexed
  2. Warn the patient: "I'm going to stroke the sole of your foot — it may feel uncomfortable"
  3. Use the blunt handle of the hammer or a key
  4. Apply firm, continuous pressure from the lateral heel, along the lateral sole, then curve medially toward the ball of the foot under the toes
  5. The stroke should take 2–3 seconds — not too fast, not too slow
ResponseNameMeaning
Toes curl down (plantarflex)Flexor plantar responseNormal in adults
Big toe extends upward + other toes fan outExtensor response = Babinski signUMN lesion (corticospinal tract above S1)
Equivocal / withdrawalRecord as suchNot diagnostic

Abdominal Reflexes (T7–T12)

  1. With the patient supine, use a pointed object to stroke from the lateral abdomen toward the midline in each quadrant
  2. Normal: Umbilicus moves toward the quadrant stroked
  3. Absent unilaterally above umbilicus (T8–T9) but present below: Spinal cord lesion at T8–T9
  4. Absent ipsilaterally: UMN lesion above that level
  5. Absent in obesity and post-abdominal surgery — not always pathological

4G. PRIMITIVE REFLEXES (Frontal Release Signs)

Present in normal infants, reappear in frontal lobe disease / diffuse cortical damage:
ReflexHow to ElicitPositive ResponseSignificance
Grasp reflexStroke the patient's palm between thumb and index with your fingersPatient involuntarily grabs your fingersFrontal lobe disease
Suck reflexTouch the centre of the lips with a tongue bladeSucking movementBilateral frontal disease
Palmomental reflexBriskly scratch the thenar eminence diagonallyIpsilateral chin mentalis muscle contractsFrontal/corticobulbar disease
Snout reflexTap the philtrum (above upper lip)Pursing of lipsFrontal disease


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STEP 5 — COORDINATION

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5A. PRINCIPLES

  • Coordination tests the cerebellar system (vermis = truncal/gait; hemispheres = limb)
  • Only meaningful if the patient has adequate power (MRC ≥ 3) and adequate sensation
  • Weakness and sensory loss cause incoordination that is NOT cerebellar — always interpret in context

5B. UPPER LIMB COORDINATION

Finger-to-Nose Test

Step-by-step:
  1. Hold your index finger at the patient's arm's length away, slightly off-centre
  2. Ask: "Touch the tip of your nose with your index finger, then touch my finger — and keep going back and forth"
  3. After several cycles, move your finger to a new position without warning
  4. The patient must reach accurately to the new position each time
  5. Observe for:
    • Dysmetria: Past-pointing (overshooting) or under-shooting the target
    • Intention tremor: Tremor that increases as the finger approaches the target (absent at rest)
    • Decomposition of movement: Movement breaks into jerky segments

Rapid Alternating Movements (Dysdiadochokinesia)

Method 1:
  1. Ask the patient to tap the back of one hand alternately with the palm and dorsum of the other hand as rapidly as possible
  2. Observe for rhythm, regularity, and speed
Method 2:
  1. Ask the patient to tap their index finger to the thumb repeatedly at speed
  2. Compare both hands
Abnormal: Slow, irregular, clumsy alternation = dysdiadochokinesia → cerebellar hemisphere lesion (ipsilateral)

5C. LOWER LIMB COORDINATION

Heel-Knee-Shin Test

Step-by-step:
  1. Patient lies supine, legs flat
  2. Ask: "Lift your right heel and place it on your left knee"
  3. Then: "Now slide your heel smoothly down your shin toward your ankle"
  4. Return to start and repeat several times
  5. Observe for:
    • Accuracy of placing heel on knee
    • Smoothness of sliding down the shin (should be in a straight line)
    • Deviations / wobbling off the shin
    • Slowing of initiation
Normal: Smooth, controlled, straight line heel slide Abnormal (cerebellar): Wobbly, irregular, deviates off the shin

Foot Tapping

  • Ask patient to tap the foot (heel on floor, foot tapping up and down) as fast and regularly as possible
  • Compare both sides — unilateral slowing = ipsilateral cerebellar or contralateral UMN

5D. CEREBELLAR SIGNS SUMMARY

SignTestCerebellar Feature
DysmetriaFinger-nose, heel-knee-shinIpsilateral hemisphere
Intention tremorFinger-noseIpsilateral hemisphere
DysdiadochokinesiaRapid alternating movementsIpsilateral hemisphere
Ataxic gaitTandem walking, watching gaitVermis (midline)
Truncal ataxiaSitting balance, Romberg-likeVermis
NystagmusOcular examinationVestibulocerebellum / brainstem
DysarthriaSpeech assessmentCerebellar connections


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STEP 6 — GAIT AND BALANCE

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6A. PRINCIPLES

Gait integrates the entire neurological system — cerebellar, pyramidal, extrapyramidal, sensory, vestibular, and musculoskeletal. Always test gait even if the patient needs minimal assistance.

6B. HOW TO ASSESS GAIT — STEP BY STEP

Environment: A corridor of at least 6–10 metres. Ensure safety — walk alongside the patient.
Step 1 — Normal walking:
  1. Ask the patient to walk to the end of the corridor and back
  2. Observe from behind initially, then from the side
  3. Assess:
    • Stride length (normal vs. short steps)
    • Base width (narrow normal vs. wide-based)
    • Arm swing — normally symmetrical
    • Posture — upright vs. stooped
    • Rhythm and regularity
    • Turning — normal vs. turns en bloc (Parkinson's)
    • Foot clearance — does the foot drag? Does the toe drop?
Step 2 — Heel walking:
  • Walk on heels down the corridor
  • Tests L4/L5 (tibialis anterior — dorsiflexion)
  • Inability = footdrop / L5 weakness
Step 3 — Tiptoe walking:
  • Walk on tiptoes
  • Tests S1 (gastrocnemius — plantarflexion)
  • Inability = S1 weakness
Step 4 — Tandem walking (heel-to-toe):
  • Walk in a straight line placing each foot directly in front of the other
  • This is the most sensitive test for cerebellar ataxia (small abnormalities not visible in normal walking)
  • Patient holds arms out if needed for balance
Step 5 — Romberg Test:
  1. Ask the patient to stand with feet together, arms by their sides
  2. Observe stability with eyes open first
  3. Then ask the patient to close their eyes
  4. Stand close to prevent falls
ResultMeaning
Stable with eyes open AND closedNormal
Unstable with eyes OPENCerebellar or vestibular problem (visual compensation fails to help)
Stable eyes open, unstable eyes closed (positive Romberg)Proprioceptive / dorsal column loss — patient relies on vision to compensate
Important: A positive Romberg is NOT a cerebellar test — it is a sign of sensory ataxia (posterior column / peripheral nerve proprioception failure). Cerebellar ataxia is present with eyes OPEN and does not worsen dramatically on closing.
Sharpened/Tandem Romberg test
Sharpened Romberg — tandem stance with arms crossed, examiner standing behind for safety

6C. SPECIFIC GAIT PATTERNS — DETAILED RECOGNITION

1. Hemiplegic Gait (UMN — unilateral)

  • What you see: Affected arm held flexed and adducted; affected leg extended and stiff, swings in a semicircle outward (circumduction) to clear the floor
  • Arm swing: Absent on affected side
  • Cause: Contralateral cortical or capsular lesion, stroke

2. Spastic ("Scissor") Gait (UMN — bilateral)

  • What you see: Both legs stiff, adducted, knees brush against each other ("scissors"), short shuffling steps on tiptoe
  • Cause: Bilateral UMN — bilateral cortical lesions, cervical myelopathy, cerebral palsy

3. Steppage (Footdrop) Gait (LMN)

  • What you see: Exaggerated hip and knee flexion to lift the foot off the ground; foot slaps down on landing; toe drags otherwise
  • Cause: L4/L5 radiculopathy, common peroneal nerve palsy, Charcot-Marie-Tooth
Steppage gait — footdrop compensation
Steppage gait — high knee lift to compensate for ankle dorsiflexion weakness / footdrop

4. Waddling Gait (Proximal muscle weakness)

  • What you see: Trunk sways side-to-side; "duck-like"; pelvis drops on the unsupported side (Trendelenburg sign)
  • Cause: Proximal myopathy (muscular dystrophy), hip girdle weakness

5. Parkinsonian Gait (Extrapyramidal)

  • What you see:
    • Stooped posture, head and trunk flexed forward
    • Shuffling, very small steps (marche à petit pas)
    • Reduced/absent arm swing bilaterally
    • Festination: Progressively faster, shorter steps — patient accelerates involuntarily
    • Start hesitation: Difficulty initiating movement
    • Freezing: Feet appear glued to the floor, especially in doorways
    • Turning en bloc: Cannot pivot; turns in multiple small steps
  • Cause: Parkinson's disease, Parkinson-plus syndromes

6. Cerebellar (Ataxic) Gait

  • What you see: Wide-based, unsteady, staggering — patient sways erratically; like a drunk person
  • Not improved by opening eyes (unlike sensory ataxia)
  • Difficulty or impossible with tandem walking
  • Cause: Cerebellar vermis lesion (alcohol, MS, tumour, stroke)

7. Sensory Ataxic Gait (Posterior column)

  • What you see: Wide-based, stamping / high-stepping gait; patient watches the floor; markedly worse in the dark or with eyes closed
  • Cause: Posterior column lesion (B12 deficiency, tabes dorsalis, sensory neuropathy)

8. Antalgic Gait (Pain-related)

  • Rapid transfer of weight off the painful limb; shortened stance phase on affected side


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INTEGRATION TABLE — UMN vs LMN vs CEREBELLAR

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FeatureUMN LesionLMN LesionCerebellar
WastingMild (disuse)Severe, earlyNone
FasciculationsAbsentPresentAbsent
ToneSpasticity (clasp-knife)FlaccidityHypotonia
PowerPyramidal pattern weaknessFocal / distal / proximalNormal or mild
ReflexesHyperreflexiaHyporeflexia / absentNormal or diminished
Plantar responseExtensor (Babinski +)Flexor or absentFlexor
CoordinationAffected only by weaknessAffected only by weaknessSeverely impaired
GaitHemiplegic / spasticSteppage / waddlingWide-based ataxic

Sources: Harrison's Principles of Internal Medicine, 22e; Textbook of Family Medicine, 9e; Adams and Victor's Principles of Neurology, 12e; Bradley and Daroff's Neurology in Clinical Practice

tone assessment properly grades then spastiity and itsgrades

Finding Sources
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Modified Ashworth Scale spasticity grading muscle tone assessment passive movement

Reading File
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Tardieu scale spasticity catch angle velocity stretch reflex assessment

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clonus ankle sustained beats upper motor neuron spasticity testing

Now I have comprehensive textbook content from Adams & Victor's (12e), Harrison's (22e), and Localization in Clinical Neurology (8e). Here is the complete, exhaustive answer.

TONE ASSESSMENT & SPASTICITY — COMPLETE DETAILED GUIDE


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PART 1 — MUSCLE TONE: WHAT IT IS

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Tone is defined as the resistance of a muscle to passive stretch at rest.
It reflects the activity of the:
  • Stretch reflex arc (muscle spindle → Ia afferent → alpha motor neuron → muscle)
  • Supraspinal control (corticospinal, reticulospinal, vestibulospinal tracts)
"Tone is the resistance of a muscle to passive stretch. Increased tone may be of several types." — Harrison's Principles of Internal Medicine, 22e

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PART 2 — HOW TO ASSESS TONE PROPERLY (STEP BY STEP)

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GOLDEN RULES BEFORE YOU START

  1. The patient must be completely relaxed — this is the single most critical requirement
  2. Distract the patient — talk to them, ask a question, have them name days of the week — this prevents voluntary muscle bracing
  3. Move joints at varying speeds and in unpredictable directions — prevents anticipatory voluntary movement
  4. Never announce what you are about to do next
  5. Always compare left vs. right at every joint
  6. Assess proximal → distal systematically

STEP 1 — POSITIONING

RegionPatient Position
Upper limbsSeated or supine, arms resting naturally
Lower limbsSupine, legs extended and relaxed
NeckSupine, head on pillow
Tell the patient: "I'm going to move your limbs for you — please don't help me and don't resist me. Just let your arm/leg go completely floppy."

STEP 2 — UPPER LIMB TONE ASSESSMENT

A. Wrist Pronation/Supination

  1. Cradle the patient's forearm with your non-dominant hand
  2. Grip their hand as if shaking hands with your dominant hand
  3. Pronate and supinate the wrist repeatedly at varying, unpredictable speeds
  4. Feel the resistance through your grip
  5. Normal: Slight, yielding spring-like resistance

B. Wrist Flexion/Extension

  1. Cup the dorsum of the patient's hand in your palm
  2. Flex and extend the wrist through full range
  3. Vary speed — slow then fast
  4. Key: At fast speed, spasticity reveals itself (velocity-dependent catch)

C. Elbow Flexion/Extension

  1. Support the forearm; grasp the wrist
  2. Flex and extend the elbow through full range
  3. Vary speed — first slow, then fast
  4. In spasticity: resistance is felt prominently in extension (flexors of UL are antigravity muscles and are spastic)

D. Shoulder

  1. Hold the upper arm gently
  2. Internally and externally rotate the shoulder
  3. Gently abduct the arm
  4. Useful for detecting shoulder rigidity in Parkinson's

STEP 3 — LOWER LIMB TONE ASSESSMENT

A. Leg Roll Test (best screening test)

  1. Patient lies supine, both legs extended flat
  2. Place both your hands on top of the patient's thigh
  3. Briskly roll the leg inward and outward (internal/external rotation at the hip)
  4. Watch the foot — it should oscillate loosely and freely
  5. Normal: Foot swings freely like a pendulum
  6. Increased tone: Foot moves rigidly with the leg — little or no foot oscillation

B. Knee Lift Test (Harrison's method)

  1. Place both hands behind the patient's knee
  2. Rapidly and briskly lift the knee upward off the table
  3. Watch the heel:
What You SeeInterpretation
Heel drags along the table for several centimetres before liftingNormal tone
Heel lifts immediately with the knee — no drag at allIncreased tone (spasticity)
Heel stays on the table even when you lift fullyDecreased tone (flaccidity/hypotonia)

C. Ankle Dorsiflexion

  1. Support the ankle with one hand under the heel
  2. With your other hand, slowly then quickly dorsiflex the foot
  3. Compare slow vs. fast — spasticity is velocity-dependent; rigidity is not

D. Clonus Testing (always test when you suspect increased tone)

Ankle clonus:
  1. Support the knee in slight flexion with one hand
  2. With the other hand, grip the sole of the foot
  3. Apply a sudden, sustained dorsiflexion jerk — hold the position firmly
  4. Count the rhythmic beats (contractions) of the calf muscle
Patellar clonus:
  1. Leg extended flat
  2. Grasp the patella between your index finger and thumb
  3. Push it sharply downward and sustain the push
  4. Feel for rhythmic oscillation under your fingers
Clonus FindingsSignificance
No beatsNormal
1–2 unsustained beatsEquivocal — may be normal
3–4 beatsBorderline
≥5 sustained beatsPathological clonus — UMN lesion

STEP 4 — RECORDING TONE

Always document:
  • Which limb(s) are affected
  • Type of abnormality (spasticity / rigidity / flaccidity / paratonia)
  • Distribution (proximal, distal, hemibody, generalised)
  • Severity (mild / moderate / severe or use a grading scale)
  • Clonus (present/absent, sustained/unsustained, number of beats)

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PART 3 — TYPES OF ABNORMAL TONE (COMPLETE)

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TYPE 1 — SPASTICITY

"Spasticity is the increase in tone associated with disease of upper motor neurons. It is velocity dependent, has a sudden release after reaching a maximum (the 'clasp-knife' phenomenon), and predominantly affects the antigravity muscles." — Harrison's, 22e
Mechanism: Loss of cortical/reticulospinal inhibition → disinhibition of the stretch reflex arc → excessive spindle afferent activity → abnormal resistance to passive stretch
Key features:
  • Velocity-dependent — faster stretch = more resistance (this is the hallmark)
  • Clasp-knife character — initial catch then sudden release, like closing a penknife
  • Predominantly affects antigravity muscles:
    • Upper limb flexors (elbow flexors, wrist flexors, finger flexors)
    • Lower limb extensors (quadriceps, plantarflexors)
  • Associated with hyperreflexia, Babinski sign, clonus
  • Develops days to weeks after acute UMN lesion (initially flaccid in acute phase)
Distribution in the body:
  • UL: Shoulder adductors, elbow flexors, wrist/finger flexors, pronators
  • LL: Hip extensors/adductors, knee extensors, ankle plantarflexors/invertors
Clinical appearance of established spasticity:
  • Upper limb: adducted shoulder, flexed elbow, pronated forearm, flexed wrist and fingers
  • Lower limb: extended knee, plantarflexed/inverted ankle, extended hip
Spastic hand deformities — flexor posturing UMN lesion
Spastic hand deformities: flexor posturing at wrist and fingers from UMN lesion

TYPE 2 — RIGIDITY

"Rigidity is hypertonia that is present throughout the range of motion (a 'lead pipe' or 'plastic' stiffness) and affects flexors and extensors equally." — Harrison's, 22e
Mechanism: Extrapyramidal (basal ganglia) dysfunction → excessive output via reticulospinal/vestibulospinal tracts → increased gamma motor neuron activity
Key features:
  • NOT velocity-dependent — resistance is the same whether you move fast or slow
  • Equal in both flexors and extensors throughout the full range of motion ("plastic")
  • "Lead pipe" feel — like bending a soft metal rod
  • Does NOT have a clasp-knife give
  • Associated with bradykinesia, tremor (Parkinson's), not with hyperreflexia
Cogwheel Rigidity:
  • Rigidity + superimposed ratchet-like interruptions = cogwheeling
  • Best felt at the wrist during pronation/supination
  • Caused by tremor superimposed on rigidity
  • To unmask: ask the patient to move the contralateral hand while you test — reinforcement makes cogwheeling appear
Cause: Parkinson's disease, Parkinson-plus syndromes (MSA, PSP)

TYPE 3 — PARATONIA (GEGENHALTEN)

"Paratonía (or gegenhalten) is increased tone that varies irregularly in a manner seemingly related to the degree of relaxation, present throughout the range of motion, and affects flexors and extensors equally." — Harrison's, 22e
Key features:
  • Patient seems to involuntarily resist movement regardless of instruction to relax
  • Resistance is inconsistent and irregular — varies moment to moment
  • Cannot be overcome by reassurance or distraction
  • Affects both directions of movement
Cause: Frontal lobe disease, severe bilateral cerebral disease, advanced dementia

TYPE 4 — FLACCIDITY / HYPOTONIA

"Weakness with decreased tone (flaccidity) occurs with disorders of motor units." — Harrison's, 22e
Key features:
  • No resistance to passive movement — limb feels heavy and dead
  • Limb drops if unsupported
  • Heel drag test: heel stays on table even when you lift fully
  • Leg roll test: foot flops excessively
  • Associated with: hyporeflexia/areflexia, wasting, fasciculations
Causes:
  • LMN lesion (anterior horn cell, root, peripheral nerve)
  • Primary muscle disease (myopathy, myositis)
  • Cerebellar disease (mild hypotonia)
  • Acute UMN lesion (spinal shock — initially flaccid before spasticity develops)
  • Neuromuscular junction disease (myasthenia gravis)

COMPARISON TABLE — ALL TONE TYPES

FeatureSpasticityRigidityCogwheelParatoniaFlaccidity
Velocity-dependentYes (key feature)NoNoNoN/A
Clasp-knifeYesNoNoNoNo
Muscles affectedAntigravity (flexors UL, extensors LL)All equallyAll equallyAll equallyAll
Quality of resistanceCatch then sudden giveUniform, plasticRatchet-likeIrregular, variableNone
ReflexesHyperreflexiaNormalNormalVariableHyporeflexia/absent
BabinskiExtensor (+)AbsentAbsentVariableAbsent
WastingMild (disuse)NoneNoneNoneSevere
TremorNoOftenYes (superimposed)NoNo
CauseUMN (corticospinal)ExtrapyramidalParkinson'sFrontal lobeLMN/muscle/acute UMN

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PART 4 — SPASTICITY GRADING SCALES

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There are two major clinical scales used to grade spasticity:

SCALE 1 — MODIFIED ASHWORTH SCALE (MAS)

The Most Widely Used Clinical Scale

What it measures: Resistance to passive movement — grades the subjective feel of tone
How to perform:
  1. Patient relaxed, limb in the starting position
  2. Move the limb through its full range of motion at a consistent, moderate speed (approximately 1 second to complete the movement)
  3. For elbow spasticity: Move from full flexion to full extension in 1 second
  4. For wrist: Move from full flexion to full extension in 1 second
  5. For ankle: Move from full plantarflexion to dorsiflexion in 1 second
  6. Feel the resistance throughout the movement and grade as below

MODIFIED ASHWORTH SCALE — FULL GRADING

GradeDescriptionWhat You Feel
0No increase in muscle toneLimb moves freely through full range — no resistance felt at all
1Slight increase in muscle tone — a catch and release OR minimal resistance at the end of range of motionYou feel a very brief, small "catch" at one point in the range, then it releases — OR slight resistance only in the last few degrees
1+Slight increase in tone — catch followed by resistance throughout the remainder (less than half) of the rangeYou feel a catch, then the resistance persists through less than half of the remaining range
2More marked increase in tone through most of the range of motion, but affected part(s) easily movedResistance is present through more than half of the range, but the limb can still be moved through full range without great effort
3Considerable increase in muscle tone — passive movement difficultYou can still move the limb but it requires significant effort throughout the range
4Affected part(s) rigid in flexion or extensionLimb cannot be moved passively — it is fixed/frozen in position

MAS Practical Example — Elbow Flexors

GradeWhat the examiner experiences moving the arm from flexion to extension
0Arm extends smoothly from 0° to 180° — no resistance
1Brief catch felt at ~130°, then gives way — rest of movement is free
1+Catch at ~120°, resistance persists until ~90°, then releases
2Resistance felt from 120° all the way through to 30°, but you can complete extension
3Stiff through entire range — you must force the extension; very difficult
4Elbow fixed in flexion — cannot be passively extended at all
Modified Ashworth Scale — passive elbow extension assessment
MAS assessment — elbow flexed (Panel A) then passively extended (Panel B), feeling resistance throughout
MAS with EMG correlation
Clinical MAS evaluation with sEMG electrode monitoring — correlating passive movement resistance with muscle electrical activity

SCALE 2 — MODIFIED TARDIEU SCALE (MTS)

More Physiologically Valid — Captures Velocity-Dependence

The Tardieu Scale specifically tests the velocity-dependent nature of spasticity — the defining pathophysiological feature — making it more accurate than the Ashworth Scale.
What it measures: The angle at which the catch occurs (R1) compared to the full passive range (R2)
The key concept: Spasticity Angle = R2 − R1 (the larger this difference, the more severe the spasticity)

THE THREE VELOCITIES

VelocitySymbolDescriptionPurpose
V1As slow as possibleGravity alone moves the limbMeasures full passive range (R2) — no reflex, just contracture component
V2Speed of limb falling under gravityNatural speedIntermediate
V3As fast as possibleFaster than natural dropElicits maximum stretch reflex — measures catch angle (R1)

MODIFIED TARDIEU SCALE — QUALITY OF MUSCLE REACTION (X Score)

GradeDescription
0No resistance throughout passive movement
1Slight resistance throughout — no clear catch at a specific angle
2Clear catch at a specific angle, followed by release
3Clonus — less than 10 seconds when maintained pressure applied
4Sustained clonus — more than 10 seconds when pressure maintained
5Joint is immovable

HOW TO PERFORM THE TARDIEU SCALE — STEP BY STEP

Example: Ankle plantarflexors (most common site tested)
Step 1 — Measure R2 (full passive range) at V1:
  1. Patient supine, knee slightly flexed (isolates soleus) or extended (isolates gastrocnemius)
  2. Move foot very slowly (gravity-assisted, no stretch reflex activated)
  3. Take the ankle from full plantarflexion to maximum dorsiflexion without resistance from spasticity
  4. Record the angle of full passive range = R2
Step 2 — Measure R1 (catch angle) at V3:
  1. Same starting position
  2. Move the foot as fast as possible — faster than the natural speed of falling
  3. Note the angle at which you feel the catch (sudden resistance from stretch reflex)
  4. Record this angle = R1
Step 3 — Calculate the Spasticity Angle:
Spasticity Angle = R2 − R1
  • Large angle (e.g. R2=30°, R1=0°, angle=30°): Significant spasticity
  • Small angle (near zero): Mild or no spasticity
  • If R1 = R2: No velocity-dependent component — suggests contracture rather than spasticity
Modified Tardieu Scale — ankle assessment with IMU sensors
Modified Tardieu Scale setup — knee extended for gastrocnemius (A) and knee flexed for soleus (B), IMU sensors measuring angular velocity at time of catch

MAS vs. MTS — WHICH TO USE?

FeatureModified Ashworth ScaleModified Tardieu Scale
Ease of useVery easyModerate
Time required1–2 min per limb5–10 min per limb
Velocity-dependent testingNo — single speed onlyYes — tests multiple velocities
Distinguishes spasticity from contractureNoYes (R1 vs. R2)
Inter-rater reliabilityModerateModerate–good
Clinical useRoutine assessment, everyday practiceResearch, rehabilitation planning, botulinum toxin decisions
Best forScreening, monitoringPrecise quantification
Recommendation:
  • Use MAS for routine clinical assessment and monitoring progress
  • Use MTS when planning botulinum toxin injections, surgery, or when contracture vs. spasticity needs to be distinguished

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PART 5 — SPASTICITY vs. CONTRACTURE (CRITICAL DISTINCTION)

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FeatureSpasticityContracture
CauseNeural — abnormal stretch reflexNon-neural — fibrosis, shortening of muscle/tendon
Velocity-dependentYesNo — same resistance at all speeds
Tardieu R1 vs. R2R1 < R2 (large difference)R1 = R2 (no difference)
ReversiblePartially (botulinum toxin, baclofen, physio)Fixed — requires surgery/serial casting
AshworthAny gradeAny grade (cannot distinguish)

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PART 6 — CONSEQUENCES OF SEVERE SPASTICITY

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Untreated severe spasticity leads to:
  • Contractures — fixed shortening of muscles and tendons
  • Joint deformities — equinovarus foot, hip adductor scissoring, flexed elbow
  • Pressure sores — from abnormal posture and immobility
  • Pain — from sustained muscle overactivity
  • Flexor/extensor spasms — especially with spinal cord lesions
  • Bladder/bowel dysfunction (in spinal lesions with severe spasms)
  • Functional loss — inability to dress, transfer, walk, use hands
Severe chronic spasticity — bilateral equinovarus deformity
Fixed bilateral equinovarus deformity — end-stage consequence of untreated ankle plantarflexor spasticity

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SUMMARY QUICK REFERENCE

══════════════════════════════════════

TONE ASSESSMENT
│
├── NORMAL → Slight spring-like resistance
│
├── INCREASED
│   ├── SPASTICITY → Velocity-dependent, clasp-knife, UMN
│   │   Grade with: MAS (0–4) or MTS (R1/R2 + quality 0–5)
│   │
│   ├── RIGIDITY → Velocity-independent, plastic/lead-pipe, extrapyramidal
│   │   + Cogwheeling → Parkinson's (rigidity + tremor)
│   │
│   └── PARATONIA → Irregular, variable, frontal lobe disease
│
└── DECREASED
    └── FLACCIDITY / HYPOTONIA → LMN, myopathy, acute UMN (shock)

Sources: Harrison's Principles of Internal Medicine, 22e; Adams and Victor's Principles of Neurology, 12e; Localization in Clinical Neurology, 8e
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