I now have enough textbook context and background to compose a comprehensive CNS case sheet. Let me compile it from Bradley and Daroff's Neurology in Clinical Practice plus standard clinical medicine framework.
CNS Case Sheet — Medicine Postings
Central Nervous System: Detailed History Taking & Examination Proforma
SECTION 1 — PATIENT IDENTIFICATION
| Field | Details |
|---|
| Name | |
| Age / Sex | |
| IP/OP No. | |
| Ward / Bed No. | |
| Occupation | |
| Address | |
| Informant | (Patient / Relative / Bystander) — Reliability: |
| Date of Admission | |
| Date of Examination | |
SECTION 2 — CHIEF COMPLAINTS
(In patient's own words, in chronological order with duration)
- _____________ — since ___________
- _____________ — since ___________
- _____________ — since ___________
SECTION 3 — HISTORY OF PRESENTING ILLNESS
General Pointers
- Mode of onset: Sudden / Acute / Sub-acute / Chronic / Insidious
- Progression: Static / Progressive / Relapsing-remitting / Stepwise
- Course: Improving / Worsening / Fluctuating
A. Headache (if present)
- Site: Unilateral / Bilateral / Holocranial / Occipital / Frontal / Peri-orbital
- Onset: Sudden ("thunderclap") / Gradual
- Character: Throbbing / Pressing / Band-like / Stabbing / Boring
- Severity: Mild / Moderate / Severe (VAS scale 1–10)
- Duration: Seconds / Minutes / Hours / Days
- Radiation: Neck / Face / Shoulder / Back
- Time of occurrence: Early morning / Nocturnal / Continuous
- Aggravating factors: Bending forward, coughing, straining, physical activity, light, noise
- Relieving factors: Rest, analgesics, darkness, sleep
- Associated features: Nausea/vomiting, photophobia, phonophobia, aura, visual changes, fever, neck stiffness
- Prior history of similar headache: Yes / No
B. Seizures / Fits (if present)
- Type of onset: Focal / Generalised / Unknown
- Aura: Rising epigastric sensation / Visual / Auditory / Olfactory / Déjà vu / Fear (note: mesial temporal auras = rising epigastric sensation; occipital = elementary visual; lateral temporal = auditory)
- Motor manifestations: Tonic / Clonic / Tonic-clonic / Myoclonic / Atonic
- Lateralisation: Unilateral / Bilateral / Head/eye deviation (direction)
- Automatisms: Lip smacking / Oro-alimentary / Hand automatisms / Bipedal / Verbal
- Duration of episode
- Loss of consciousness: Yes / No
- Post-ictal state: Confusion / Headache / Todd's palsy / Sleepiness / Duration
- Tongue bite / Urinary/faecal incontinence
- Frequency: per day / week / month
- Precipitants: Sleep deprivation / Alcohol / Fever / Stress / Menstruation / Flashing lights
- Risk factors: Febrile seizures in infancy, meningitis/encephalitis (especially before age 5), head trauma, family history (Bradley & Daroff)
C. Loss of Consciousness / Altered Sensorium
- Onset: Sudden / Gradual
- Duration
- Preceding symptoms: Prodrome, warning
- Depth: GCS at time of event
- Associated: Seizures, injuries, incontinence, cyanosis
- Recovery: Complete / Partial / Time to recovery
D. Weakness / Paralysis
- Distribution: Monoplegia / Hemiplegia / Paraplegia / Tetraplegia / Diplegia
- Onset: Sudden (stroke) / Progressive (tumour, motor neurone disease) / Episodic
- UMN vs LMN features in history: Stiffness and spasticity (UMN) vs floppiness and wasting (LMN)
- Progression: Fixed / Ascending (Guillain-Barré) / Descending
- Associated sensory loss: Yes / No / Level
- Bladder and bowel involvement
- Diurnal variation: Morning stiffness / End-of-day fatigue (myasthenia)
E. Sensory Symptoms
- Type: Numbness / Tingling / Paraesthesia / Pain / Burning / Electric shocks
- Distribution: Dermatomal / Peripheral nerve / "Stocking-glove" / Hemibody / Saddle area
- Loss of specific modalities: Pain/temperature vs vibration/joint position sense
- Lhermitte's sign (electric shock on neck flexion — demyelination)
- Trophic changes, pressure sores
F. Visual Symptoms
- Blurring: Monocular (anterior to chiasm) / Binocular
- Diplopia: Horizontal / Vertical / Oblique; worse at distance vs near
- Visual field defects: Hemianopia / Quadrantanopia / Tunnel vision / Central scotoma
- Transient visual loss (amaurosis fugax)
- Oscillopsia / Visual obscurations / Photopsia
G. Speech and Language
- Dysarthria: Slurring / Nasal / Scanning / Explosive / Low volume
- Dysphasia/Aphasia: Expressive (Broca's — non-fluent) / Receptive (Wernicke's — fluent) / Global
- Dysphonia: Hoarseness
- Dysphagia: Solids / Liquids / Both
H. Gait and Balance
- Type: Wide-based (cerebellar/sensory ataxia) / Steppage / Scissor / Spastic / Festinant / High-stepping / Waddling
- Falls: Frequency, direction (retropulsion in Parkinsonism)
- Dizziness / Vertigo: True vertigo (rotational) vs light-headedness; positional
I. Involuntary Movements
- Type: Tremor / Chorea / Athetosis / Ballismus / Myoclonus / Tics / Dystonia / Fasciculations
- For tremor: Rest (Parkinsonism) / Action (Essential tremor) / Intention (cerebellar)
- Relation to posture, activity, sleep
J. Cognitive and Behavioural Symptoms
- Memory: Short-term / Long-term deterioration
- Orientation: Time / Place / Person
- Language deterioration
- Personality change / Disinhibition / Apathy
- Sleep disturbance: Insomnia / Hypersomnia / REM behaviour disorder
- Hallucinations: Visual / Auditory / Tactile
K. Autonomic Symptoms
- Bladder: Frequency / Urgency / Retention / Incontinence
- Bowel: Constipation / Incontinence
- Sweating: Hyperhidrosis / Anhidrosis
- Postural dizziness (orthostatic hypotension)
- Sexual dysfunction
SECTION 4 — PAST HISTORY
| System | Details |
|---|
| Similar episodes | Yes / No |
| Hypertension | Yes / No; duration, drugs |
| Diabetes mellitus | Yes / No; duration, control |
| Cardiac disease | IHD / AF / RHD / Prosthetic valves |
| Stroke / TIA | Yes / No; residual deficit |
| Epilepsy | Yes / No; onset age, drugs |
| Meningitis / Encephalitis | Yes / No; age at occurrence |
| Head injury / Spine injury | Yes / No; nature |
| Tuberculosis | Yes / No; treatment |
| HIV / Immunosuppression | Yes / No |
| Surgical procedures | Yes / No |
| Blood transfusions | Yes / No |
| Drug allergies | |
SECTION 5 — FAMILY HISTORY
- Similar neurological illness in family members (epilepsy, migraine, muscular dystrophy, Huntington's, spinocerebellar ataxia)
- Three-generation pedigree if hereditary condition suspected (Bradley & Daroff)
- Consanguinity: Yes / No
- Neurodegenerative disorders (Parkinson's, Alzheimer's, Friedreich's ataxia)
- Sudden unexplained death
SECTION 6 — PERSONAL HISTORY
| Item | Details |
|---|
| Diet | Vegetarian / Non-vegetarian / Nutritional deficiencies |
| Appetite | Normal / Decreased / Increased |
| Sleep | Normal / Disturbed |
| Bowel/Bladder | Normal / Altered |
| Smoking | Yes / No; pack-years |
| Alcohol | Yes / No; type, quantity, duration; withdrawal symptoms |
| Illicit drugs | Yes / No; type, route |
| Occupation | Exposure to toxins (lead, mercury, organophosphates) |
| Marital history | |
| Travel history | Endemic areas (neurocysticercosis, malaria cerebral, rabies) |
SECTION 7 — TREATMENT HISTORY
- Current medications (especially antiepileptics, antihypertensives, anticoagulants, steroids, immunosuppressants)
- Previous neurological treatments and response
- Herbal / OTC medications
SECTION 8 — SOCIOECONOMIC & DEVELOPMENTAL HISTORY (Paediatric cases)
- Birth: Full-term / Premature; birth weight; mode of delivery
- Perinatal: Asphyxia, NICU stay, neonatal seizures
- Developmental milestones: Head control / Sitting / Standing / Walking / First words / Sentences
- School performance
- Immunisation history
- Regression of milestones: Yes / No
SECTION 9 — GENERAL PHYSICAL EXAMINATION
Vitals
| Parameter | Value |
|---|
| Pulse | /min; rhythm; volume; character |
| Blood Pressure | mmHg (both arms; lying and standing) |
| Respiratory Rate | /min |
| Temperature | °F / °C |
| SpO₂ | % |
| GCS | E__ V__ M__ = __ /15 |
General Examination
- Built and nourishment: Good / Poor
- Pallor / Icterus / Cyanosis / Clubbing / Lymphadenopathy / Oedema
- Skin: Café-au-lait spots / Ash-leaf macules / Shagreen patches / Port wine stain / Neurofibromas (neurocutaneous markers)
- Head circumference (paediatric): Microcephaly / Macrocephaly
- Spine: Kyphosis / Scoliosis / Hairy patch / Spina bifida / Sacral dimple
- Neck stiffness: Kernig's sign / Brudzinski's sign (meningeal irritation)
SECTION 10 — SYSTEMIC EXAMINATION
Cardiovascular: (embolic sources)
- Murmurs, AF, peripheral pulses, carotid bruits
Respiratory:
- Consolidation, effusion (TB, paraneoplastic)
Abdomen:
- Hepatosplenomegaly (storage disorders, Wilson's disease)
- Liver: cirrhosis (hepatic encephalopathy)
SECTION 11 — NEUROLOGICAL EXAMINATION
A. HIGHER MENTAL FUNCTIONS (Cortical Functions)
1. Consciousness
- GCS: Eyes (1–4) / Verbal (1–5) / Motor (1–6)
- AVPU: Alert / Voice / Pain / Unresponsive
2. Orientation
- Time (day, date, month, year, time of day)
- Place (hospital, ward, city, country)
- Person (own name, examiner)
3. Attention and Concentration
- Digit span (forward ≥6, backward ≥4)
- Serial 7s subtraction from 100
- Months of year backwards
4. Memory
- Immediate: Digit repetition
- Short-term (recent): 3-object recall at 5 minutes
- Long-term (remote): Past events, autobiographical
5. Language
| Test | Finding |
|---|
| Spontaneous speech | Fluent / Non-fluent |
| Comprehension | Intact / Impaired (simple and complex commands) |
| Repetition | Intact / Impaired ("no ifs, ands, or buts") |
| Naming | Intact / Anomia (confrontation naming) |
| Reading | Intact / Alexia |
| Writing | Intact / Agraphia |
Localisation: Broca's (area 44/45, frontal) = non-fluent + intact comprehension; Wernicke's (area 22, temporal) = fluent + impaired comprehension; Conduction = fluent + impaired repetition
6. Praxis
- Ideomotor: Mimic brushing teeth, combing hair, salute
- Ideational: Use a key, fold a letter, light a match
- Constructional: Copy a figure (intersecting pentagons)
7. Visuospatial and Gnosia
- Clock drawing test
- Neglect: Line bisection, cancellation test
- Prosopagnosia / Object agnosia
8. Frontal Lobe Functions
- Abstraction (similarities/proverbs)
- Judgement
- Wisconsin card sorting / MMSE / MoCA (document score)
- Perseveration / Utilisation behaviour
B. CRANIAL NERVE EXAMINATION
| CN | Nerve | Test | Finding |
|---|
| I | Olfactory | Coffee/soap — each nostril separately | N / Anosmia / Hyposmia |
| II | Optic | Visual acuity (Snellen), visual fields (confrontation), colour vision, fundoscopy | Papilloedema / Optic atrophy |
| III | Oculomotor | Ptosis, pupil size + light reflex + accommodation, EOM (up/down/medial) | CN III palsy |
| IV | Trochlear | Downgaze in adduction | Superior oblique palsy |
| V | Trigeminal | Facial sensation (all 3 divisions), corneal reflex, jaw opening + deviation, jaw jerk | |
| VI | Abducens | Lateral gaze | Lateral rectus palsy |
| VII | Facial | Facial symmetry at rest + on movement; taste anterior 2/3 tongue | UMN (forehead spared) vs LMN (Bell's palsy) |
| VIII | Vestibulocochlear | Whisper test, Rinne, Weber; nystagmus; Romberg with eyes closed | |
| IX/X | Glossopharyngeal / Vagus | Palate movement (say "aah"), uvula deviation, gag reflex, voice quality | Bulbar vs Pseudobulbar |
| XI | Accessory | Sternocleidomastoid (head turning), trapezius (shoulder shrug against resistance) | |
| XII | Hypoglossal | Tongue at rest (fasciculations?), protrusion (deviation to side of lesion in LMN) | |
C. MOTOR SYSTEM
1. Inspection
- Wasting / Hypertrophy (muscle bulk)
- Fasciculations (LMN, lower motor neurone)
- Involuntary movements
2. Tone
- Upper limbs: Clasp-knife spasticity (UMN) / Lead-pipe or cogwheel rigidity (extrapyramidal) / Hypotonia (LMN / cerebellar) / Gegenhalten (frontal)
- Lower limbs: Clonus — ankle / patellar (≥3 beats = pathological)
3. Power (MRC Grade)
| Grade | Description |
|---|
| 0 | No contraction |
| 1 | Visible contraction only |
| 2 | Movement with gravity eliminated |
| 3 | Movement against gravity only |
| 4 | Movement against resistance (reduced) |
| 5 | Normal power |
Test each group: shoulder, elbow, wrist, fingers (grip, opposition); hip, knee, ankle, toe
4. Reflexes
Deep Tendon Reflexes (DTR)
| Reflex | Root | Right | Left |
|---|
| Biceps | C5,C6 | | |
| Supinator | C5,C6 | | |
| Triceps | C7 | | |
| Knee (Patellar) | L3,L4 | | |
| Ankle (Achilles) | S1,S2 | | |
Grade: 0 = absent, + = diminished, ++ = normal, +++ = brisk, ++++ = clonus
Plantar Response (Babinski sign)
- Right: Flexor / Extensor (UMN sign) / Equivocal
- Left: Flexor / Extensor / Equivocal
Superficial Reflexes
- Abdominal reflex: Upper (T8–T10) / Lower (T10–T12) — absent in UMN lesions
- Cremasteric reflex (males): L1–L2
Primitive Reflexes (if frontal lobe disease suspected)
- Palmomental / Grasp / Snout / Rooting / Glabellar tap
D. SENSORY SYSTEM
(Always examine with eyes closed; test distal before proximal; compare sides)
| Modality | Pathway | Test | Findings |
|---|
| Pain (pinprick) | Spinothalamic | Disposable pin | |
| Temperature | Spinothalamic | Hot/cold tubes | |
| Light touch | Both | Cotton wool | |
| Vibration | Dorsal column | 128 Hz tuning fork on bony prominences | |
| Joint position sense (proprioception) | Dorsal column | Passive movement of distal phalanx | |
| Two-point discrimination | Cortical | Calipers | |
| Stereognosis | Cortical | Identify coin/key by feel | |
| Graphaesthesia | Cortical | Trace number on palm | |
Sensory Level (if spinal cord lesion suspected): Mark highest level of normal sensation on trunk
Dissociated sensory loss: Pain/temperature loss with preserved vibration/JPS = syringomyelia / Brown-Séquard
E. CEREBELLAR SYSTEM
(DANISH — Dysdiadochokinesia, Ataxia, Nystagmus, Intention tremor, Scanning speech, Hypotonia)
| Test | Finding |
|---|
| Finger-nose test | Dysmetria / Intention tremor / Past-pointing |
| Heel-shin test | Dysmetria |
| Diadochokinesia (rapid alternating movements) | Dysdiadochokinesia |
| Romberg test | Positive in sensory ataxia; negative in cerebellar ataxia |
| Tandem gait (heel-to-toe) | Inability = cerebellar |
| Nystagmus | Direction; horizontal / vertical / rotatory |
| Speech | Scanning / Staccato / Explosive |
| Rebound phenomenon | Positive in cerebellar disease |
F. GAIT EXAMINATION
| Gait Type | Features | Localisation |
|---|
| Hemiplegic / Spastic | Circumduction, arm adducted | Contralateral cortex / capsule |
| Scissors gait | Both legs spastic, crossed | Bilateral UMN |
| Cerebellar (ataxic) | Wide-based, staggering, cannot tandem | Cerebellum |
| Sensory ataxic | Wide-based, worse in dark, Romberg + | Dorsal columns |
| Steppage | High-stepping (foot drop) | Peripheral nerve / LMN |
| Festinant | Small shuffling steps, stooped, retropulsion | Basal ganglia (Parkinsonism) |
| Waddling | Bilateral hip girdle weakness | Myopathy |
| Antalgic | Protective (pain-related) | Musculoskeletal |
G. AUTONOMIC EXAMINATION
- Postural BP (lying → standing; drop >20 mmHg systolic = orthostatic hypotension)
- Bladder distension
- Sweating asymmetry (Homer's — ipsilateral anhidrosis)
- Horner's syndrome: Ptosis + Miosis + Anhidrosis + Enophthalmos (sympathetic chain)
H. MENINGEAL SIGNS
| Sign | Technique | Positive if |
|---|
| Neck stiffness | Passive neck flexion | Resistance to chin-chest approximation |
| Kernig's sign | Hip 90° flexed → extend knee | Pain/spasm at <135° |
| Brudzinski's sign | Flex neck | Involuntary hip/knee flexion |
| Jolt accentuation | Rotate head horizontally 2–3 Hz | Headache worsens |
I. SPINE EXAMINATION (if cord/radiculopathy suspected)
- Straight leg raise (SLR): ° at which pain reproduces; Lasègue sign
- Femoral stretch test: L2–L4 roots
- Spinal tenderness / Para-spinal muscle spasm
- Percussion over vertebrae
SECTION 12 — PROVISIONAL DIAGNOSIS
Anatomical Localisation (answer these in order):
- Which level? — Cortex / Subcortex / Brainstem / Cerebellum / Spinal cord / Peripheral nerve / Neuromuscular junction / Muscle
- Which side? — Left / Right / Bilateral / Crossed (brainstem)
- UMN vs LMN?
- Single lesion vs multiple lesions?
Provisional Diagnosis: ___________________________________________
Differential Diagnoses:
-
-
-
SECTION 13 — INVESTIGATIONS
Routine
- CBC, ESR / CRP
- Blood glucose (RBS/FBS/HbA1c)
- Renal function tests, Electrolytes (Na, K, Ca, Mg)
- Liver function tests
- Lipid profile
- Thyroid function tests (TSH, T3, T4)
- Urine routine + microscopy
Neuroimaging
- CT Brain: Non-contrast first (haemorrhage, calcification); contrast (abscess, tumour)
- MRI Brain ± Spine: DWI (acute infarct), FLAIR (periventricular lesions), T1+Gad, MRA/MRV
- CT Angiography / MR Angiography: Vascular lesions
CSF Analysis (after ruling out raised ICP)
| Parameter | Normal | Significance |
|---|
| Opening pressure | 70–200 mm H₂O | Raised in meningitis, SAH, IIH |
| Colour / Appearance | Colourless, clear | Xanthochromia = SAH; turbid = bacterial meningitis |
| Cells | 0–5 lymphocytes/mm³ | Pleocytosis |
| Protein | 15–45 mg/dL | Elevated in GBS, MS, infections |
| Glucose | >60% of blood glucose | Low in bacterial/TB/fungal |
| Gram stain, Culture/Sensitivity | | |
| AFB stain / ADA | | TB meningitis |
| India ink stain | | Cryptococcus |
| Oligoclonal bands | Absent | Multiple sclerosis |
Electrophysiology
- EEG: Epilepsy, encephalopathy
- Nerve conduction studies (NCS) + EMG: Peripheral neuropathy, myopathy, NMJ disorder
- Visual/Brainstem/Somatosensory Evoked Potentials
Special Investigations (targeted)
- Serum B12, Folate, Thiamine
- VDRL/TPHA (neurosyphilis)
- HIV ELISA
- ANA, Anti-dsDNA, ANCA, Anti-phospholipid antibodies (vasculitis, lupus)
- Paraneoplastic antibodies (anti-Hu, anti-Yo, anti-NMDAR)
- Urine porphyrins
- Serum ceruloplasmin + 24h urine copper (Wilson's disease)
- Muscle enzymes: CPK, LDH, aldolase
SECTION 14 — MANAGEMENT PLAN
Immediate (Emergency):
- Airway, Breathing, Circulation
- GCS < 8 → Consider intubation
- Seizure → IV Lorazepam → Phenytoin loading
Short-term:
- Disease-specific treatment
- Supportive: IV fluids, nasogastric feeding if dysphagia, pressure sore prevention, DVT prophylaxis, catheterisation if retention
Long-term / Rehabilitation:
- Physiotherapy, Occupational therapy, Speech therapy
- Antiepileptic therapy, Antiplatelets/anticoagulants, Neuroprotection
- Bowel and bladder care
- Psychological support / Counselling
SECTION 15 — PROGNOSIS & DISCUSSION
- Natural history of the condition
- Complications anticipated
- Disability assessment
- Discussion of case with supervisor
- Correlation of clinical features with investigations
QUICK LOCALISATION GUIDE (Aide-mémoire)
| Feature | Lesion Location |
|---|
| Contralateral hemiplegia + hemisensory loss | Internal capsule |
| Hemiplegia + hemianopia + aphasia (dominant) | MCA territory |
| Crossed CN palsy + contralateral hemiplegia | Brainstem |
| Bilateral pyramidal signs + sensory level | Spinal cord |
| Ascending paralysis, areflexia, albuminocytological dissociation | GBS (peripheral nerve) |
| Ptosis + diplopia + fatiguable weakness | Neuromuscular junction (Myasthenia gravis) |
| Proximal weakness + wasting, no sensory loss | Myopathy |
| Cerebellar signs + ipsilateral Horner's | Lateral medullary (Wallenberg) syndrome |
| Resting tremor + cogwheel rigidity + festinant gait | Basal ganglia (Parkinsonism) |
| Dysdiadochokinesia + nystagmus + scanning speech | Cerebellar |
Sources: Bradley and Daroff's Neurology in Clinical Practice, 8th Ed. | Clinical Medicine, Medicine Postings Standard Framework.
This case sheet covers the full CNS history-taking and examination workflow for medicine postings. Key points to remember:
- Localise before diagnosing — always answer: which level, which side, UMN or LMN, single or multiple lesion
- Aura type guides temporal lobe localisation (rising epigastric = mesial temporal; elementary visual = occipital)
- Risk factors for epilepsy include febrile status epilepticus in infancy, early meningitis/encephalitis, and head trauma — all correlate with specific pathologies
- Meningeal signs must always be tested in headache + fever presentations
- CSF analysis after ruling out raised ICP via fundoscopy or neuroimaging