CNS examination in detail for MD medicine resistant based on standards book

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CNS Examination in Detail

Based on: Adams and Victor's Principles of Neurology, 12th Edition; Bradley and Daroff's Neurology in Clinical Practice; Harrison's Principles of Internal Medicine 22E

Overview and Approach

The neurological examination begins before the patient reaches the examination table - observations during the waiting room, the walk to the room, and history-taking all yield diagnostic information. Lack of facial expression (hypomimia) may suggest parkinsonism; a worried or astonished expression may suggest progressive supranuclear palsy; ptosis suggests myasthenia gravis or a brainstem lesion. Speech patterns may reveal dysarthria, aphasia, or spasmodic dysphonia.
The full neurological examination systematically covers every CNS region, peripheral nerve, muscle, sensory modality, and reflex. In practice, a screening examination is combined with a focused examination directed by the history.

I. MENTAL STATUS EXAMINATION

A. Level of Consciousness and Attention

The first and most fundamental assessment. Graded as:
  • Alert - fully awake and responsive
  • Drowsy/Somnolent - arousable by verbal stimuli
  • Stupor - arousable only by vigorous/painful stimuli
  • Coma - unarousable
Bedside attention tests:
  • Digit Span Test - Forward: read digits at 1/sec, patient repeats; Normal = 7 ± 2 digits. Backward: Normal = 5 ± 1
  • Serial Subtraction - Subtract 7s from 100 (100, 93, 86...) or 3s; tests concentration
  • "A" Vigilance Test - Tap each time letter "A" is heard in a random letter sequence
  • Palm-Side-Fist sequence - Three-step motor sequence (frontal lobe function)

B. Orientation

Test orientation to:
  • Time: Date, day, month, year, time of day (off by >3 days on date or >4 hours on time = significantly disoriented)
  • Place: Hospital/clinic, type of place, city
  • Person: Own name (rarely lost except in severe dementia)

C. Memory

TypeTest
Immediate recallRepeat 3 words immediately
Short-term (recent) memoryRecall 3 words after 5 minutes
Remote memoryHistorical facts, past personal events
EpisodicRecall of specific dated personal events
Also test: Registration of examiner's name; day-to-day recollection of recent incidents; dates of hospitalization.

D. Language

If aphasia is suspected, test all modalities:
ComponentTest
Spontaneous speechFluency, content, word-finding
Comprehension"Point to the window," execute commands
RepetitionRepeat "no ifs, ands, or buts"
NamingName objects, parts of objects (anomia)
ReadingAloud and for comprehension
WritingSpontaneous and to dictation
SpellingSpell simple words forward/backward
Note: Distinguish the language of confusion (inattentive, with intrusions, perseverations) from true aphasia (consistent pattern of language breakdown).

E. Praxis (Motor Planning)

  • Commanded and imitated gestures: hammering a nail, blowing out a candle, throwing dice
  • Sequential hand positions (Luria three-step: fist-edge-palm)
  • Dressing apraxia: observed while patient dresses

F. Visuospatial Function / Gnosis

  • Clock drawing test: Draw clock face, place numbers, set time to 10 past 11
  • Line bisection: Bisect a horizontal line (neglect = bisects off-center)
  • Copy figures: Pentagon intersection, cube
  • Floor plan drawing: Sketch layout of own home
  • Object recognition (Gnosis): Name objects by sight, by touch (stereognosis), by sound

G. Executive Function and Judgment

  • Abstract reasoning: Interpret proverbs ("A rolling stone gathers no moss")
  • Similarities: "In what way are an apple and an orange alike?"
  • Judgment: "What would you do if you found a stamped, addressed envelope on the street?"
  • Insight into own illness: Does patient recognize their deficit?

H. Frontal Lobe Specific Tests

  • Go/No-Go task: Tap when examiner taps once; do not tap when examiner taps twice
  • Perseveration: Alternate sequence drawing (square-triangle-square-triangle); Luria loops
  • Grasp reflex, Palmomental reflex, Gegenhalten (paratonia)

II. CRANIAL NERVE EXAMINATION

CN I - Olfactory Nerve

Test separately for each nostril with familiar odors (coffee, vanilla, clove). Loss = anosmia.
  • Indicated in: head trauma, suspected Parkinson's disease, anterior cranial fossa lesions, meningioma.

CN II - Optic Nerve

  1. Visual Acuity - Snellen chart at 6 metres (20 feet) for each eye separately; pinhole corrects refractive error; near card (Rosenbaum) for bedside
  2. Visual Fields - Confrontation testing (each eye tested separately, examiner's face as central fixation point); count fingers or wiggling fingers in four quadrants; for detailed mapping - perimetry/Goldman fields
  3. Color vision - Ishihara plates (sensitive for optic nerve disease)
  4. Fundoscopy - Optic disc (pallor, papilloedema, cupping), vessels, macula

CN III, IV, VI - Oculomotor, Trochlear, Abducens

  1. Pupillary examination:
    • Size (normal 2-5 mm), shape, symmetry
    • Direct and consensual light reflex (afferent = CN II, efferent = CN III)
    • Swinging flashlight test - RAPD (relative afferent pupillary defect) = optic nerve or severe retinal disease
    • Near reflex (accommodation-convergence)
    • Anisocoria: >1 mm difference - test in light and dark (Horner vs CN III)
  2. Eye movements:
    • Saccades: rapid voluntary movements ("Look left/right quickly")
    • Smooth pursuit: follow slowly moving finger (H-pattern)
    • Vergence: convergence
    • Vestibulo-ocular reflex (VOR): doll's head maneuver
    • Nystagmus: direction, type (horizontal/vertical/torsional), fast vs slow phase
  3. Ptosis: CN III (complete, with pupil dilation) vs Horner's (partial, with miosis, anhidrosis)

CN V - Trigeminal Nerve

  1. Sensation - Test pinprick and light touch in all three divisions (V1 ophthalmic, V2 maxillary, V3 mandibular) bilaterally; also test cornea
  2. Corneal reflex - Touch cornea gently with wisp of cotton; normal = bilateral blink (afferent CN V1, efferent CN VII); come from side to avoid visual stimulus
  3. Motor division - Jaw strength: clench teeth (masseter/temporalis bulk), open jaw against resistance (pterygoids); jaw deviates to weak side on opening
  4. Jaw jerk - Tap chin with finger; brisk = upper motor neuron lesion above pons

CN VII - Facial Nerve

  1. Observe at rest, during speech and spontaneous smiling (subtle weakness more evident)
  2. Upper face: Raise eyebrows (frontalis), tightly close eyes (resist opening - orbicularis oculi)
  3. Lower face: Puff cheeks, whistle, show teeth (smile to command), purse lips
  4. Upper vs Lower motor neuron distinction: UMN (central) lesion spares forehead due to bilateral cortical innervation; LMN (Bell's palsy) involves entire ipsilateral hemiface
  5. Taste: Anterior 2/3 tongue (chorda tympani, branches of CN VII) - sweet, salt, sour on tongue tip
  6. Hyperacusis: Loud sounds perceived more intensely (stapedius muscle paralysis - LMN CN VII)

CN VIII - Vestibulocochlear

Cochlear (hearing):
  1. Whispered voice test: Whisper 2-syllable words at 60 cm behind each ear separately
  2. Rinne test: 512 Hz tuning fork - compare air conduction (ear canal) vs bone conduction (mastoid); Normal/SNHL: AC > BC (Rinne positive); Conductive loss: BC > AC (Rinne negative)
  3. Weber test: Vibrating fork on center of forehead; lateralizes to better ear in SNHL; lateralizes to worse ear in conductive loss
  4. Formal audiometry if abnormality detected
Vestibular:
  1. Romberg test: Feet together, arms at sides; maintain balance eyes open then eyes closed (positive = falls with eyes closed = proprioceptive or vestibular loss)
  2. Marching test (Unterberger): March on spot with eyes closed; rotates to side of vestibular lesion
  3. Dix-Hallpike test: For BPPV
  4. Head impulse test: Rapid horizontal head thrust; corrective saccade = vestibular hypofunction

CN IX & X - Glossopharyngeal and Vagus

  1. Phonation: Ask "aah" - observe soft palate elevation; deviates to normal side if unilateral weakness; bilateral weakness = nasal voice, regurgitation
  2. Gag reflex: Touch posterior pharyngeal wall or tonsillar pillar - afferent IX, efferent X; reduced in lower motor neuron lesions
  3. Swallowing: Observe for coughing, nasal regurgitation; CN X lesion causes dysphagia
  4. Voice quality: Hoarseness or bovine cough = recurrent laryngeal nerve (CN X) lesion

CN XI - Accessory Nerve

  1. Sternocleidomastoid: Turn head against resistance (turns head to contralateral side); test each separately
  2. Trapezius: Shoulder shrug against resistance; ipsilateral weakness

CN XII - Hypoglossal Nerve

  1. Tongue at rest: Observe for fasciculations, atrophy (LMN lesion)
  2. Tongue protrusion: Deviates to side of weakness (LMN) or away from lesion (UMN)
  3. Rapid tongue movements: "La-la-la" (lingual sounds)
  4. Dysarthria: "Linguo-labial" sounds affected

III. MOTOR SYSTEM EXAMINATION

A. Inspection

  • Muscle bulk: Wasting/atrophy (LMN, disuse, myopathy), hypertrophy (muscular dystrophy, hypothyroid myopathy)
  • Fasciculations: Spontaneous visible muscle twitching at rest (LMN / anterior horn cell disease)
  • Abnormal movements: Tremor (rest vs action), chorea, athetosis, ballismus, dystonia, myoclonus, tics
  • Posture at rest: External rotation of hip (UMN lesion), hemiplegic posture

B. Tone

Examine with patient relaxed; examiner passively moves limbs through full range:
  • Normal: Mild resistance to passive movement
  • Hypotonia: Reduced resistance (cerebellar, LMN, acute spinal shock, chorea)
  • Spasticity: Velocity-dependent increased resistance (pyramidal/UMN lesion); "clasp-knife" - give-way at end; greater in arm flexors and leg extensors
  • Rigidity: Uniform increased resistance throughout range (extrapyramidal); "lead-pipe" or "cogwheel" (Parkinson's - Froment's sign: cogwheeling enhanced by contralateral arm movement)
  • Gegenhalten (Paratonia): Variable resistance, mirrors examiner's pressure (frontal lobe lesion)
  • Clonus: Rhythmic oscillating contractions at sustained stretch (brisk at ankle); >5 beats = pathological

C. Power (Strength)

Use MRC Grading Scale (Medical Research Council):
GradeDescription
0No contraction
1Flicker of contraction, no movement
2Movement with gravity eliminated
3Movement against gravity but not resistance
4Movement against some resistance (4-, 4, 4+ variants)
5Normal power
Systematic muscle testing by region:
Upper Limbs:
  • Shoulder abduction (C5, deltoid), adduction (C6-8, pectoral/lat)
  • Elbow flexion (C5-6, biceps), extension (C7, triceps)
  • Wrist extension (C6-7, extensors), flexion (C6-7, flexors)
  • Finger extension (C7, extensor digitorum), flexion (C8, FDP/FDS)
  • Finger abduction/adduction (T1, interossei)
  • Thumb opposition (C8-T1, abductor pollicis brevis)
Lower Limbs:
  • Hip flexion (L1-2, iliopsoas), extension (L5-S1, gluteus maximus)
  • Hip abduction (L4-5, gluteus medius), adduction (L2-4, adductors)
  • Knee extension (L3-4, quadriceps), flexion (L5-S1, hamstrings)
  • Ankle dorsiflexion (L4-5, tibialis anterior), plantarflexion (S1-2, gastrocnemius)
  • Hallux extension (L5, EHL), toe flexion (S1-2)
Quick screening maneuvers:
  • Pronator drift: Arms outstretched, palms up, eyes closed for 10 seconds; pronation and downward drift = UMN lesion; upward drift = sensory ataxia; arm "orbiting" away = subtle weakness
  • Barre's sign (legs): Patient prone, knees bent at 90°; affected leg drifts down
  • Heel-walking, toe-walking: Foot drop (L4-5) vs S1 weakness; "rise on toes" - assess with patient standing at wall

D. Coordination (Cerebellar Function)

Upper limbs:
  • Finger-nose-finger test: Patient touches own nose then examiner's finger back and forth; look for intention tremor, dysmetria, past-pointing
  • Rapid alternating movements (Dysdiadochokinesia): Alternating pronation/supination ("patting the back of hand"), or rapidly touching each fingertip with thumb
  • Rebound test: Suddenly release flexed arm against examiner's resistance; cerebellar disease = delayed check/overshoot
Lower limbs:
  • Heel-shin test: Heel placed on opposite knee, run smoothly down shin to ankle; cerebellar disease = ataxic, irregular path
  • Foot tapping: Tap foot rapidly on examiner's hand
  • Toe-finger test
Truncal ataxia: Inability to sit upright steadily without support (midline cerebellar vermis lesion)

IV. REFLEXES

A. Deep Tendon Reflexes (Muscle Stretch Reflexes)

ReflexStimulus SiteRootResponse
BicepsBiceps tendonC5-C6Elbow flexion
Supinator (Brachioradialis)Radial styloidC5-C6Forearm supination/flexion
TricepsTriceps tendonC7-C8Elbow extension
Finger flexionExaminer's fingers on patient'sC8-T1Finger flexion
Patellar (Knee jerk)Patellar tendonL3-L4Knee extension
Achilles (Ankle jerk)Achilles tendonS1-S2Plantarflexion
Grading:
  • 0 = Absent
  • 1+ = Present only with reinforcement (Jendrassik maneuver - clasp hands and pull)
  • 2+ = Normal
  • 3+ = Brisk (may be normal)
  • 4+ = Very brisk with clonus (pathological - UMN)
Jendrassik Maneuver: Patient hooks fingers together and pulls; examiner taps lower limb reflexes simultaneously; reinforces barely obtainable reflexes.

B. Plantar Response (Babinski Sign)

  • Stroke the lateral aspect of sole from heel toward ball and across to big toe
  • Normal (flexor response): Plantar flexion of toes
  • Abnormal (Babinski sign, extensor response): Dorsiflexion of big toe ± fanning of other toes = damage to corticospinal tract (UMN)
  • Withdrawal response: Quick withdrawal of whole foot (not Babinski)
  • Triple flexion response: Flexion of hip, knee, dorsiflexion of foot (pathological, similar significance to Babinski)
Equivalent signs:
  • Oppenheim: Knuckle pressed firmly down the shin
  • Gordon: Squeezing the calf
  • Chaddock: Lateral aspect of dorsum of foot from lateral malleolus forward
  • Bing: Prick dorsum of foot with pin

C. Superficial Reflexes

  • Abdominal reflexes: Stroke skin from lateral to midline in each quadrant; reflex absent ipsilateral to pyramidal lesion; absent bilaterally in obese patients (less reliable)
  • Cremasteric reflex: Stroke inner thigh; cremasteric muscle contracts, scrotal sac rises; Lost in UMN lesions, ipsilateral cord/root lesion
  • Anal reflex: Perianal skin scratch; anal sphincter contracts; Loss = S3-S5 lower motor neuron
  • Bulbocavernosus reflex: Squeeze glans penis/tap pubic symphysis; contraction of bulbocavernosus; Loss = sacral cord/conus lesion

D. Primitive (Pathological) Reflexes

  • Grasp reflex: Stimulate palm; involuntary grasping (frontal lobe lesion)
  • Palmomental reflex: Scratch thenar eminence; ipsilateral chin muscle contracts (frontal lobe)
  • Snout reflex: Tap philtrum; pursing of lips (bilateral frontal disease)
  • Glabellar tap: Repeated taps on glabella; normal = habituates after 2-3 taps; Parkinson's = does not habituate (Myerson's sign)
  • Rooting and sucking reflexes: Normally present in infants; return in severe dementia/frontal lobe disease

V. SENSORY EXAMINATION

Requires full patient cooperation; test one side against the other; move from area of reduced sensation outward.

A. Primary (Modality-Specific) Sensations

ModalityPathwayTest
PainSpinothalamic (contralateral)New disposable pin; sharp vs dull
TemperatureSpinothalamic (contralateral)Cold (metal tuning fork) vs warm; or test tubes
VibrationPosterior column (ipsilateral)128 Hz tuning fork on bony prominences (toes, medial malleolus, tibial crest, knee, ASIS, fingers, wrist, elbow, shoulder)
Proprioception (Joint position sense - JPS)Posterior column (ipsilateral)Move distal phalanx up or down with fingers on lateral sides; start distally (toes, fingers); normal = detect small movements
Light touchPosterior column + spinothalamicWisp of cotton; compare sides

B. Cortical Sensory Modalities

(Require intact primary sensation; lesion in parietal cortex)
  • Stereognosis: Identify common objects (key, coin, pen) placed in hand without looking
  • Graphesthesia: Identify numbers or letters written on palm
  • Two-point discrimination: Minimum distance for perceiving two distinct touch stimuli; fingertip normal = 2-5 mm; loss = parietal lesion
  • Sensory extinction (double simultaneous stimulation): Touch both sides simultaneously; patient reports only one side (extinction/neglect = parietal lobe, usually non-dominant)
  • Point localization: Patient points to where examiner touches with eyes closed

C. Patterns of Sensory Loss

PatternLesion Site
Glove-and-stockingPeripheral neuropathy (dying-back)
DermatomalNerve root (radiculopathy)
Dissociated (pain/temp lost, vibration/JPS intact)Spinothalamic only: syringomyelia, Brown-Sequard
Contralateral hemibody (all modalities)Internal capsule/thalamus
Ipsilateral body + contralateral faceLateral medullary syndrome (Wallenberg)
Saddle distributionCauda equina lesion
Cortical sensory loss with normal primary sensationParietal lobe lesion

VI. GAIT AND STATION

Observe the patient rising from a chair (proximal muscle strength), and then:
Gait TypeFeaturesLocalization
HemiplegicArm flexed, adducted; leg circumductsCorticospinal (contralateral)
Scissors (Spastic-bilateral)Both legs stiff, cross in frontBilateral corticospinal
Steppage (foot drop)High-step, foot slaps floor; cannot heel-walkL4-5, peroneal nerve
Trendelenburg (waddling)Pelvis dips to opposite side on stepHip abductors (L4-5, S1)
Cerebellar ataxicWide-based, reeling, irregular; falls to side of lesionCerebellum/cerebellar tracts
Sensory ataxicWide-based, high-stepping, "stamping"; worsens eyes closed (Romberg +)Posterior columns / peripheral neuropathy
ParkinsonianShuffling small steps; stooped; reduced arm swing; festination; en-bloc turnsBasal ganglia
Apraxic (Magnetic)"Feet glued to floor"; small shuffling steps; normal on lyingFrontal lobe (NPH, frontal mass)
AntalgicShortened stance phase on painful limbMusculoskeletal
Romberg Test: Stand with feet together, eyes open (tests cerebellar function) then eyes closed (proprioception). Positive = significant sway/falling with eyes closed = sensory ataxia (posterior column / large-fiber neuropathy). A cerebellar patient sways with eyes both open and closed.
Tandem (heel-to-toe) Gait: Unmasks subtle cerebellar or vestibular imbalance.
Hopping/one-leg stand: Detects unilateral weakness or imbalance.

VII. SCREENING NEUROLOGICAL EXAMINATION (Quick Reference)

(From Bradley & Daroff's Table 1.1 and Adams & Victor Table 1-4)
ComponentKey Tests
Mental StatusOrientation, memory (3-word recall), language (spontaneous speech, naming), attention (serial 7s)
CN ISmell (if indicated: trauma, Parkinson's)
CN IIVisual acuity, confrontation fields, fundoscopy, pupil reactions
CN III, IV, VIEye movements (H-pattern), pupils, nystagmus
CN VPin/touch on face, corneal reflex
CN VIIRaise brows, close eyes tightly, smile to command
CN VIIIWhisper test, Rinne & Weber
CN IX-XPalate elevation, gag, voice quality
CN XIShoulder shrug, head turn
CN XIITongue protrusion, fasciculations
MotorTone, power (proximal and distal), pronator drift, heel/toe walk
ReflexesBiceps (C5-6), triceps (C7), supinator (C6), knee (L3-4), ankle (S1), plantars
CoordinationFinger-nose-finger, heel-shin, rapid alternating movements
SensoryPin, vibration, joint position sense (fingers and toes)
Gait/StationObservation, Romberg, tandem walk

VIII. SPECIAL EXAMINATION CONSIDERATIONS

Meningeal Signs

  • Neck stiffness (Nuchal rigidity): Passive neck flexion resisted; chin-to-chest test; indicates meningeal irritation (meningitis, subarachnoid hemorrhage)
  • Kernig's sign: Flex hip to 90° then extend knee - resistance/pain at <135° = positive
  • Brudzinski's sign: Passive neck flexion causes involuntary hip and knee flexion
  • Jolt accentuation: Horizontal head rotation at 2-3 Hz worsens headache = meningitis

Signs of Raised Intracranial Pressure

  • Papilloedema on fundoscopy
  • Sixth nerve palsy (false localizing sign)
  • Cushing's triad: bradycardia, hypertension, irregular respiration

Upper vs Lower Motor Neuron Differentiation

FeatureUMN (Central)LMN (Peripheral)
ToneSpastic (clasp-knife)Flaccid (hypotonia)
WeaknessPyramidal pattern (extensors in arm, flexors in leg)Distribution of nerve/root/muscle
ReflexesBrisk, clonusReduced/absent
PlantarExtensor (Babinski)Flexor
FasciculationsAbsentPresent
WastingLate, disuse onlyEarly, prominent
Abdominal reflexesAbsentPresent

Sources

  • Adams and Victor's Principles of Neurology, 12th Edition - Chapter 1 (Approach to the Patient with Neurologic Disease), pp. 18-21
  • Bradley and Daroff's Neurology in Clinical Practice - Chapter 1 (Neurological Examination), Table 1.1
  • Harrison's Principles of Internal Medicine, 22nd Edition - Mental Status Examination section

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What's inside (12 pages)

PageSectionContents
1CoverFull navy/teal design with 8-section index
2Mental StatusConsciousness grading, attention tests, orientation, memory types, language components, praxis, visuospatial, frontal tests
3Cranial NervesAll 12 CNs - technique, key finding, localisation; RAPD test; Rinne/Weber interpretation table
4Motor SystemInspection, tone types (spasticity/rigidity/clonus), MRC 0-5 scale, upper + lower limb muscle testing with roots & nerves
5Motor cont.Screening manoeuvres (pronator drift, Barré, heel/toe walk), coordination tests (DANISH mnemonic)
6ReflexesDTR table with roots, grading 0-4+, Jendrassik, Babinski technique + equivalents (Oppenheim, Gordon, Chaddock, Bing), superficial reflexes
7SensoryPrimary modalities with pathways, cortical sensory tests, 8-pattern localisation table
8Gait & Station10 gait patterns with features and localisation, Romberg test, additional station tests
9Special SignsUMN vs LMN differentiation table, meningeal signs (Kernig, Brudzinski, jolt), raised ICP signs, autonomic examination
10-11Quick Screens10-point bedside neurological screen, key mnemonics (cranial nerves, dermatomes, aphasia types)
12ReferencesAdams & Victor 12e, Bradley & Daroff, Harrison's 22e, DeMyer's

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Localisation of stroke according to history and cns examination findings

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