CENTRAL NERVOUS SYSTEM EXAMINATION
I. HISTORY TAKING POINTS
1. Chief Complaints Analysis
When patient reports:
a) Weakness
-
Character: Flaccid, spastic, fatigable, episodic
- Flaccid → LMN lesion, Peripheral neuropathy, Guillain-Barré syndrome
- Spastic → UMN lesion (Stroke, MS, Myelopathy)
- Fatigable → Myasthenia Gravis
- Episodic → Periodic paralysis, Multiple sclerosis
-
Site:
- Hemibody → Stroke, Cortical lesion
- Quadriparesis → High cervical cord lesion, Brainstem
- Distal weakness → Peripheral neuropathy, Motor neuron disease
- Proximal weakness → Myopathy, Muscular dystrophy
-
Severity:
- Rapid progression → Stroke, GBS
- Slowly progressive → MND, Muscular dystrophy
- Relapsing-remitting → Multiple sclerosis
b) Sensory disturbances
-
Character: Numbness, tingling, burning, shooting pain
- Burning → Peripheral neuropathy (diabetes)
- Shooting → Root compression, Sciatica
- Loss of vibration/proprioception → Posterior column involvement
-
Site:
- Glove & stocking → Peripheral neuropathy
- Dermatomal → Nerve root lesion
- Hemisensory → Thalamic stroke
- Sensory level → Spinal cord lesion
-
Severity/Progression:
- Sudden onset → Infarct
- Gradual → Tumor, Degeneration
c) Headache
-
Character: Throbbing, dull, lancinating, band-like
- Throbbing → Migraine
- Dull, continuous → Tension headache, Tumor
- Early morning with vomiting → Raised ICP
-
Site:
- Unilateral → Migraine, Cluster
- Occipital → Cervical spondylosis, Posterior fossa tumor
-
Severity:
- Explosive onset → Subarachnoid hemorrhage
- Progressive → Tumor
d) Seizures
-
Character: Focal, Generalized, Myoclonic, Absence
- Focal → Structural lesion
- Generalized → Idiopathic epilepsy, metabolic
- Myoclonic → Juvenile myoclonic epilepsy
- Absence → Childhood absence epilepsy
-
Associated features: Aura, post-ictal confusion (Focal onset), tongue bite, incontinence
e) Gait disturbances
- Type:
- Hemiplegic gait → UMN lesion
- Spastic gait → Paraplegia, Cord lesion
- Ataxic gait → Cerebellar lesion
- Festinant gait → Parkinsonism
- High-stepping → Peripheral neuropathy
f) Visual disturbances
- Character: Blurring, diplopia, field defects, transient vision loss
- Blurring → Optic neuritis
- Diplopia → Brainstem lesion, CN palsy
- Field defects → Optic chiasm lesion (Bitemporal hemianopia)
g) Speech disturbances
- Aphasia → Cortical (dominant hemisphere)
- Dysarthria → Brainstem, CN lesion
- Nasal voice → Palatal paralysis
h) Cognitive or Behavioral changes
- Acute confusion → Encephalopathy
- Chronic decline → Dementia, Frontal lobe lesion
- Personality change → Frontal lobe tumor, Pick's disease
i) Vertigo
- Peripheral: Severe, positional, with hearing loss (Labyrinthitis)
- Central: Mild, persistent, with ataxia (Cerebellar stroke)
j) Autonomic dysfunction
- Orthostatic hypotension → Autonomic neuropathy
- Bladder dysfunction → Spinal cord involvement
2. Past History
- Stroke, HTN, DM → Vascular causes
- Trauma → Epidural/subdural hematoma
- TB, HIV → Meningitis, Tuberculoma
- Cancer → Paraneoplastic syndrome, brain metastasis
3. Family History
- Huntington’s, Parkinson’s, Ataxia → Genetic predisposition
- Epilepsy → Genetic or structural predisposition
4. Personal History
- Alcohol → Cerebellar degeneration, Wernicke’s encephalopathy
- Smoking → Vascular risk, Stroke
5. Occupational/Environmental History
- Heavy metals → Encephalopathy
- Rural residence → Neurocysticercosis
II. CLINICAL EXAMINATION POINTS (with diagnostic interpretation)
1. General Examination
-
Neurocutaneous markers:
- Café-au-lait spots → Neurofibromatosis
- Ash leaf macules → Tuberous sclerosis
-
Involuntary movements at rest → Parkinsonism, Chorea
2. Higher Mental Function Examination
Consciousness level
- Drowsy, Comatose → Diffuse brain dysfunction (Trauma, Metabolic, Meningitis)
Orientation
- Disorientation → Delirium, Dementia
Memory disturbance
- Immediate → Attention deficit
- Recent → Hippocampal lesion
- Remote → Diffuse cortical dysfunction
Language
- Fluent aphasia → Wernicke’s area lesion
- Non-fluent → Broca’s area lesion
- Global aphasia → Large MCA infarct
Apraxia, Agnosia
- Apraxia → Dominant parietal lesion
- Agnosia → Occipital/parietal lobe
Frontal lobe dysfunction
- Disinhibition, impaired judgment
3. Cranial Nerve Examination
II - Optic nerve
- Visual field defects:
- Bitemporal hemianopia → Pituitary tumor
- Homonymous hemianopia → Contralateral occipital/parietal lesion
III, IV, VI
- Diplopia, ptosis → Brainstem lesion, raised ICP
V
- Facial numbness → Trigeminal neuralgia, pontine lesion
VII
- UMN palsy → Forehead sparing
- LMN palsy → Bell’s palsy
VIII
- Sensorineural deafness → Acoustic neuroma
- Nystagmus → Vestibular dysfunction
IX, X
- Nasal voice, dysphagia → Brainstem lesion
XI
- Shoulder droop → Accessory nerve lesion
XII
- Tongue deviation → Ipsilateral LMN lesion, Contralateral UMN lesion
4. Motor System Examination
Bulk
- Wasting → LMN lesion
- Hypertrophy → Pseudohypertrophy in Duchenne
Tone
- Spasticity → UMN lesion
- Rigidity → Parkinsonism
- Hypotonia → LMN, Cerebellar lesion
Power
- Hemiparesis → Stroke
- Distal weakness → Neuropathy
- Proximal weakness → Myopathy
Involuntary movements
- Tremor:
- Rest → Parkinsonism
- Intention → Cerebellar
- Postural → Essential tremor
Reflexes
- Exaggerated → UMN lesion
- Absent → LMN lesion
- Plantar upgoing → Pyramidal tract lesion
Coordination
- Dysmetria, intention tremor → Cerebellar
- Dysdiadochokinesia → Cerebellar
Cranial Nerve Examination – Detailed
I – Olfactory Nerve
Tests:
- Ask patient to close eyes & occlude one nostril. Present a non-irritant odor (coffee, vanilla, peppermint)
- Ask to identify the smell. Repeat on both sides.
Interpretation:
- Anosmia (loss of smell) → Trauma (cribriform plate fracture), Meningioma, Frontal lobe tumor
- Parosmia (distorted smell) → Temporal lobe epilepsy
- Hyposmia → Viral infection, aging
- Hallucinations of smell → Uncinate fits
II – Optic Nerve
Tests:
A. Visual Acuity
- Snellen’s chart (Distance)
- Jaeger’s chart (Near vision)
B. Color Vision
- Ishihara plates
C. Visual Fields
- Confrontation test
- Perimetry (Goldmann / Automated Humphrey)
D. Pupillary Reflexes
- Direct light reflex
- Consensual light reflex
- Swinging flashlight test (Relative afferent pupillary defect)
E. Fundoscopy
- Optic disc, Cup-disc ratio, Pallor, Papilledema, Retinal hemorrhages
F. Red Desaturation Test
- Tests early optic neuritis
Interpretation:
- Visual acuity ↓ → Optic neuropathy, Refractive errors
- Field defects:
- Bitemporal hemianopia → Pituitary tumor
- Homonymous hemianopia → Optic tract lesion
- Central scotoma → Optic neuritis
- Pupillary reflex abnormal → Optic nerve lesion
III, IV, VI – Oculomotor, Trochlear, Abducens Nerves
These are tested together
Tests:
A. Inspection
- Ptosis → CN III palsy, Myasthenia
B. Eye Position
- Strabismus, gaze deviation
C. Extraocular Movements (EOM)
- Ask patient to follow finger in ‘H’ pattern
D. Diplopia Charting
- Red-green glasses test
- Hess chart
E. Convergence Test
F. Nystagmus observation
G. Pupil Size and Reactivity
Interpretation:
- CN III palsy → Ptosis, ‘Down and out’ eye, Dilated pupil
- CN IV palsy → Vertical diplopia, Head tilt
- CN VI palsy → Medial deviation, inability to abduct
V – Trigeminal Nerve
Tests:
A. Sensory (V1, V2, V3 branches)
- Light touch, pain, temperature over:
- Ophthalmic
- Maxillary
- Mandibular areas
B. Corneal Reflex
- Afferent: V1
- Efferent: VII
C. Motor
- Palpate masseter & temporalis while clenching teeth
D. Jaw jerk reflex
- Exaggerated in UMN lesion
Interpretation:
- Loss of sensation in one branch → Peripheral nerve lesion
- Loss in all divisions → Brainstem lesion, pontine infarct
- Absent corneal reflex → CN V or VII lesion
- Weak muscles of mastication → LMN lesion (pons)
VII – Facial Nerve
Tests:
A. Inspection
- Facial asymmetry, forehead wrinkles, nasolabial fold
B. Motor Tests
- Ask patient to:
- Raise eyebrows
- Close eyes tightly
- Show teeth
- Puff cheeks
- Whistle
C. Taste
- Anterior 2/3rd of tongue: Sweet, salty
D. Stapedius reflex
- Hyperacusis if impaired
E. Lacrimation test
Interpretation:
- LMN lesion → Whole face affected (Bell's palsy)
- UMN lesion → Forehead spared
- Loss of taste → Chorda tympani lesion
- Hyperacusis → Stapedius muscle involvement
VIII – Vestibulocochlear Nerve
Tests:
A. Cochlear Component
- Finger rub test
- Rinne’s test: AC > BC (normal)
- Weber’s test: Lateralization in conductive loss
- Audiometry (Pure tone)
- Otoacoustic emissions
B. Vestibular Component
- Dix-Hallpike maneuver → BPPV
- Head impulse test → Vestibular hypofunction
- Romberg’s test
- Caloric test (COWS – Cold Opposite, Warm Same)
Interpretation:
- Sensorineural loss → Acoustic neuroma, Labyrinthitis
- Vertigo with nystagmus → Vestibular neuronitis, Cerebellar stroke
IX & X – Glossopharyngeal & Vagus Nerves
Tests:
A. Palatal Movement
- Ask patient to say “Ah”
- Observe uvula deviation
B. Gag Reflex
- Afferent: IX
- Efferent: X
C. Phonation
- Hoarseness, nasal voice
D. Swallowing
E. Cough reflex
Interpretation:
- Absent gag reflex → IX or X nerve lesion
- Uvula deviated away from lesion → Unilateral vagus lesion
- Nasal regurgitation → Palatal palsy
XI – Spinal Accessory Nerve
Tests:
A. Sternocleidomastoid strength
- Ask patient to turn head against resistance
B. Trapezius strength
- Shrug shoulders against resistance
Interpretation:
- Weakness → LMN lesion in posterior triangle (surgical injury) or brainstem lesion
XII – Hypoglossal Nerve
Tests:
A. Tongue Inspection
- Atrophy, fasciculations
B. Tongue Protrusion
- Deviation → Towards side of LMN lesion
C. Tongue movement
- Lateral movement, speed
Interpretation:
- Deviation towards side of lesion → LMN palsy
- UMN lesion → Contralateral weakness without atrophy
5. Sensory System Examination
Primary sensations
- Loss of vibration/proprioception → Posterior column disease
- Loss of pain/temp → Spinothalamic tract lesion
- Sensory level → Spinal cord compression
Cortical sensations
- Astereognosis → Parietal cortex lesion
6. Cerebellar Examination
- Nystagmus, Dysarthria, Ataxia → Cerebellar lesion
- Romberg positive → Sensory ataxia
7. Gait Examination
- Spastic → UMN lesion
- Ataxic → Cerebellar lesion
- High stepping → Peripheral neuropathy
- Parkinsonian → Basal ganglia disease
8. Meningeal Signs
- Neck stiffness, Kernig’s, Brudzinski’s → Meningitis, SAH
9. Autonomic Nervous System
- Orthostatic hypotension → Autonomic failure
- Bladder dysfunction → Spinal cord lesion
10. Psychiatric Evaluation
- Apathy, Disinhibition → Frontal lobe
- Delirium → Acute diffuse dysfunction
- Dementia → Alzheimer’s, Vascular, Lewy body
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