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Clinical Examination III: Neurological, eye, ENT and musculoskeletal

🩺 Clinical examination III: neurological, eye, ENT and musculoskeletal. Neurological and musculoskeletal examinations are often the most feared OSCE stations because there is a lot to do in a short time. A fixed routine helps: for neurology - inspection, tone, power, reflexes, coordination and sensation, then localise the lesion; for joints - look, feel, move, special tests, function. This chapter covers the upper and lower limb neurological examination, cranial nerves, cerebellar examination, gait, the eye and fundoscopy, ear, nose and throat, and the GALS screen and regional joint examinations.
Your four questions after a neurological examination: Is the problem upper motor neuron, lower motor neuron, sensory, cerebellar, extrapyramidal or a combination? Where is the lesion (brain, brainstem, cord, root, plexus, nerve, junction, muscle)? What is the likely pathology (vascular, inflammatory, degenerative, neoplastic, metabolic)? What investigation will confirm it?


Upper Limb Neurological Examination
  • Inspection - posture (flexed arm in hemiparesis), wasting (small muscles of the hand, shoulder girdle), fasciculations (LMN - MND), tremor, involuntary movements, scars (carpal tunnel release, neck surgery). Pronator drift - arms outstretched, palms up, eyes closed for 20–30 seconds: pronation and downward drift (UMN); upward drift (cerebellar); searching movements of fingers (pseudoathetosis - proprioceptive loss).
  • Tone - shoulder, elbow and wrist movements with the patient relaxed: spasticity (velocity-dependent, "clasp-knife" - UMN), rigidity ("lead-pipe" or "cogwheel" with tremor - extrapyramidal), hypotonia (LMN, cerebellar, acute UMN).
  • Power (MRC scale 0–5): 0 no contraction; 1 flicker; 2 movement with gravity eliminated; 3 against gravity; 4 against some resistance; 5 normal.
MovementRootNerve
Shoulder abductionC5Axillary
Elbow flexionC5–6Musculocutaneous
Elbow extensionC7Radial
Wrist extensionC6–7Radial
Finger extensionC7Radial (posterior interosseous)
Finger flexionC8Median and ulnar
Finger abduction (dorsal interossei)T1Ulnar
Thumb abduction (abductor pollicis brevis)T1Median
  • Reflexes (with reinforcement if absent - clench teeth): biceps (C5–6), supinator (C5–6), triceps (C7); Hoffmann's sign (UMN).
  • Coordination - finger–nose test (intention tremor, past-pointing - cerebellar), dysdiadochokinesia (rapid alternating movements).
  • Sensation - light touch and pinprick (spinothalamic) in dermatomes (C5 lateral upper arm, C6 thumb, C7 middle finger, C8 little finger, T1 medial forearm) and peripheral nerve territories; vibration (128 Hz tuning fork - start distally) and proprioception (dorsal columns).
Lower Limb Neurological Examination
  • Inspection - wasting, fasciculations, deformity (pes cavus - hereditary neuropathy, Friedreich's ataxia), scars, posture, gait (if safe).
  • Tone - roll the leg, lift the knee briskly (spastic leg kicks up), ankle clonus (more than 3–5 beats - UMN).
MovementRootNerve
Hip flexionL1–2Femoral (iliopsoas)
Hip extensionL5–S1Inferior gluteal
Knee extensionL3–4Femoral
Knee flexionL5–S1Sciatic
Ankle dorsiflexionL4–5Deep peroneal
Great toe extensionL5Deep peroneal
Ankle plantar flexionS1Tibial
Ankle eversionL5–S1Superficial peroneal
Ankle inversionL4–5Tibial
  • Reflexes - knee (L3–4), ankle (S1), plantar response (Babinski - extensor = UMN).
  • Coordination - heel–shin test.
  • Sensation - dermatomes (L2 anterior upper thigh, L3 anterior knee, L4 medial leg and medial malleolus, L5 dorsum of foot and great toe, S1 lateral foot and sole, S2 posterior thigh, S3–5 perianal - saddle anaesthesia); vibration (start at the great toe), proprioception, monofilament (diabetic foot).
  • Romberg's test - stands with feet together, eyes open then closed: falling with eyes closed = sensory ataxia (dorsal column or large fibre neuropathy - B12, tabes dorsalis); cerebellar patients are unsteady with eyes open.
  • Completion - "I would examine the upper limbs and cranial nerves, check for a sensory level (cord lesion), perform a rectal examination for anal tone and saddle sensation if cauda equina is suspected, and examine gait."
Localising the Lesion
FeatureUpper motor neuronLower motor neuron
WastingMinimal (disuse only)Prominent
FasciculationsNoYes
ToneIncreased (spasticity, clonus)Reduced
Weakness patternPyramidal - extensors weaker in arms, flexors in legsMuscles supplied by the root or nerve
ReflexesBriskReduced or absent
PlantarsExtensorFlexor
  • Mixed UMN and LMN signs - motor neuron disease (no sensory signs), cervical myeloradiculopathy (LMN at the level, UMN below), subacute combined degeneration (B12 - absent ankle jerks with extensor plantars), Friedreich's ataxia, conus medullaris lesion, taboparesis.
  • Patterns of sensory loss: glove and stocking (peripheral neuropathy), dermatomal (radiculopathy), single nerve territory (mononeuropathy - carpal tunnel - median), sensory level (spinal cord), dissociated (syringomyelia - "cape" loss of pain and temperature with preserved light touch; Brown-Séquard - ipsilateral weakness and dorsal column loss with contralateral spinothalamic loss), hemisensory (thalamus or cortex), crossed (brainstem - ipsilateral face, contralateral body).
  • Common peripheral nerve lesions: median at the wrist (carpal tunnel - thenar wasting, weak thumb abduction, sensory loss over lateral 3½ fingers; Phalen's and Tinel's), ulnar at the elbow (hypothenar and interosseous wasting, claw hand of ring and little fingers, Froment's sign), radial (wrist drop - Saturday night palsy), common peroneal at the fibular head (foot drop, weak dorsiflexion and eversion, preserved inversion - distinguishes from L5 radiculopathy; sensory loss over dorsum of the foot), lateral cutaneous nerve of thigh (meralgia paraesthetica).
Cranial Nerve Examination
  • I (olfactory) - ask about smell (formal testing rarely); loss with head injury, COVID-19, Parkinson's, frontal tumours.
  • II (optic) - acuity (Snellen chart, with glasses/pinhole), colour vision (Ishihara - early in optic neuritis), visual fields (confrontation; the patient covers one eye), pupils (direct and consensual light reflexes, swinging light test for a relative afferent pupillary defect - optic neuritis, optic nerve compression), accommodation, fundoscopy.
  • III, IV, VI (eye movements) - "H" pattern, ask about diplopia; III palsy - eye "down and out", ptosis, ± dilated pupil (surgical third - painful, dilated pupil - posterior communicating artery aneurysm - urgent CT angiography; medical third - pupil-sparing - diabetes, hypertension); IV - vertical diplopia worse looking down (stairs), head tilt; VI - failure of abduction (raised intracranial pressure - false localising sign); internuclear ophthalmoplegia (MS - failure of adduction with nystagmus of the abducting eye); nystagmus.
  • V (trigeminal) - sensation in V1, V2, V3; muscles of mastication (clench teeth, open jaw against resistance - deviates towards the weak side); corneal reflex (V1 afferent, VII efferent); jaw jerk (brisk in pseudobulbar palsy).
  • VII (facial) - raise eyebrows, close eyes tightly, puff cheeks, show teeth. LMN lesion - whole half of the face including forehead (Bell's palsy - prednisolone within 72 hours, eye protection; Ramsay Hunt - vesicles in the ear; parotid tumour; cholesteatoma). UMN lesion (stroke) - forehead spared (bilateral cortical supply).
  • VIII (vestibulocochlear) - whisper test, Rinne's (512 Hz fork - air conduction louder than bone normally; bone > air in conductive loss) and Weber's (lateralises to the affected ear in conductive loss, to the better ear in sensorineural loss); head impulse test, Dix–Hallpike (BPPV).
  • IX, X (glossopharyngeal, vagus) - palate movement ("ahh" - uvula deviates away from the side of a lesion), gag reflex (if indicated), voice, cough, swallow.
  • XI (accessory) - shrug shoulders (trapezius), turn head against resistance (sternocleidomastoid).
  • XII (hypoglossal) - tongue at rest (wasting, fasciculations - MND), protrusion (deviates towards the side of the lesion).
  • Bulbar (LMN) versus pseudobulbar (UMN) palsy - bulbar: wasted fasciculating tongue, absent jaw jerk, nasal speech (MND, GBS, myasthenia, brainstem stroke); pseudobulbar: spastic tongue, brisk jaw jerk, emotional lability, spastic dysarthria (bilateral strokes, MND, MS).
Cerebellar Examination and Gait
  • Cerebellar signs - "DANISH": Dysdiadochokinesia, Ataxia (gait and truncal), Nystagmus (towards the side of the lesion), Intention tremor (finger–nose), Slurred (staccato, scanning) speech, Hypotonia/heel–shin abnormality. Unilateral cerebellar lesions cause ipsilateral signs.
  • Causes - "PASTRIES": Posterior fossa tumour, Alcohol, Stroke (or MS - sclerosis), Trauma, Rare (Friedreich's ataxia, spinocerebellar ataxias, paraneoplastic - anti-Yo), Iatrogenic (phenytoin, lithium, carbamazepine), Endocrine (hypothyroidism), SOL.
GaitFeaturesCause
HemiplegicLeg stiff, circumducted, arm flexedStroke
Spastic (scissoring)Stiff, narrow-based, toes catchCord lesion, cerebral palsy, MS
ParkinsonianShuffling, small steps, reduced arm swing, stooped, festinant, difficulty turning (en bloc)Parkinson's disease
Cerebellar (ataxic)Wide-based, unsteady, falls towards the side of the lesion; cannot tandem walkCerebellar disease
Sensory ataxic (stamping)High-stepping, watches the feet, Romberg positiveDorsal column loss, peripheral neuropathy
Steppage (high-stepping)Foot drop - lifts knee high, foot slapsCommon peroneal palsy, L5 radiculopathy, CMT
WaddlingTrunk sways, pelvis drops (Trendelenburg)Proximal myopathy, hip pathology, pregnancy
AntalgicShort stance phase on the painful sideArthritis, injury
Apraxic (magnetic)Feet appear stuck to the floorNormal pressure hydrocephalus (with urinary incontinence and dementia), frontal lobe disease
Parkinsonism and Other Movement Disorders
  • Parkinsonism - bradykinesia (essential - slowness and decrement in amplitude on repetitive finger tapping) plus rigidity and/or rest tremor (4–6 Hz "pill-rolling", asymmetric, reduces with movement); postural instability later.
  • Other signs - hypomimia (mask-like face), hypophonia, micrographia, glabellar tap (Myerson's sign), shuffling gait; non-motor features (anosmia, REM sleep behaviour disorder, constipation, depression, autonomic dysfunction, dementia).
  • Parkinson-plus syndromes - progressive supranuclear palsy (vertical gaze palsy - especially downward, early falls backwards, axial rigidity), multiple system atrophy (early autonomic failure, cerebellar signs), dementia with Lewy bodies (early dementia, visual hallucinations, fluctuating cognition), corticobasal degeneration (alien limb, apraxia). Poor levodopa response.
  • Drug-induced parkinsonism - antipsychotics, metoclopramide, prochlorperazine - symmetrical, often with tremor.
  • Essential tremor - bilateral postural and action tremor of the hands (and head, voice), family history, improves with alcohol; propranolol or primidone.
  • Other movement disorders - chorea (Huntington's, Sydenham's, pregnancy, drugs), hemiballismus (subthalamic stroke), dystonia, tics, myoclonus.
Eye Examination and Fundoscopy
  • Visual acuity - Snellen chart at 6 metres (e.g. 6/6 normal; 6/60 - largest letter); pinhole improves refractive error; record each eye.
  • Visual fields - confrontation testing with a red hatpin; patterns: monocular loss (retina, optic nerve), bitemporal hemianopia (chiasm - pituitary adenoma, craniopharyngioma), homonymous hemianopia (optic tract/radiation/occipital - stroke), superior quadrantanopia (temporal lobe), inferior quadrantanopia (parietal lobe), central scotoma (optic neuritis, macular disease), tunnel vision (glaucoma, retinitis pigmentosa).
  • Pupils - size, shape, symmetry; light reflexes, RAPD. Horner's (small pupil, ptosis, anhidrosis - sympathetic chain: stroke, Pancoast, carotid dissection - painful Horner's is an emergency), Holmes–Adie (large, slowly reactive pupil, young women, absent reflexes), Argyll Robertson (small irregular pupils that accommodate but do not react to light - neurosyphilis, diabetes), third nerve palsy (dilated).
  • Fundoscopy - dim the room, ideally dilate pupils (tropicamide 1% - check for angle-closure risk); your right eye for their right eye; red reflex (absent - cataract, retinoblastoma in children), optic disc (colour, margins, cup:disc ratio - >0.5 suggests glaucoma), vessels (AV nipping, silver wiring, emboli), each quadrant of retina, macula (ask the patient to look at the light).
FindingCause
Papilloedema (swollen disc, blurred margins, loss of venous pulsation, haemorrhages)Raised intracranial pressure - tumour, IIH, venous sinus thrombosis, malignant hypertension
Optic atrophy (pale disc)Previous optic neuritis (MS), compression, glaucoma, ischaemia, B12, hereditary (Leber's)
Diabetic retinopathy - background (microaneurysms, dot and blot haemorrhages, hard exudates), pre-proliferative (cotton wool spots, venous beading), proliferative (new vessels), maculopathy (exudates near the macula)Diabetes - annual retinal screening
Hypertensive retinopathy - silver/copper wiring, AV nipping, flame haemorrhages, cotton wool spots, papilloedema (grade 4 - malignant hypertension)Hypertension
Central retinal artery occlusion - pale retina, cherry-red spotEmbolus, GCA - emergency
Central retinal vein occlusion - "stormy sunset" widespread haemorrhagesHypertension, glaucoma, hyperviscosity
Retinitis pigmentosa - bone spicule pigmentation, tunnel visionHereditary
Drusen, geographic atrophy, neovascularisationAge-related macular degeneration (wet AMD - urgent anti-VEGF)
Roth spots - haemorrhages with pale centresInfective endocarditis, leukaemia
  • Red eye red flags - reduced vision, severe pain, photophobia, irregular or fixed pupil, corneal opacity, contact lens wearer, recent eye surgery, trauma → same-day ophthalmology (acute angle-closure glaucoma, keratitis, anterior uveitis, scleritis).
Ear, Nose and Throat Examination
  • Ear - inspect the pinna and surrounding skin (scars, discharge, vesicles - Ramsay Hunt); otoscopy (pull the pinna up and back in adults, back in children; largest speculum that fits): canal (wax, otitis externa - swollen, painful; foreign body), tympanic membrane - colour, light reflex, perforation, retraction, fluid level or bubbles (glue ear), bulging red drum (acute otitis media), white keratin debris in the attic (cholesteatoma); hearing tests (whisper, Rinne, Weber).
  • Nose - external shape, septal deviation, anterior rhinoscopy (septal haematoma after trauma - drain urgently to prevent septal necrosis; polyps - grey, insensate, mobile; Little's area for epistaxis), airflow on each side (misting a metal spatula), smell.
  • Mouth and throat - with a light and tongue depressor: lips, teeth, gums, buccal mucosa, tongue (including underneath), floor of mouth, hard and soft palate, tonsils (size, exudate, asymmetry - quinsy displaces the uvula; unilateral enlargement - lymphoma or carcinoma), posterior pharyngeal wall; palpate any lesion (with gloves) and the salivary glands (parotid, submandibular - bimanual for stones).
  • Neck - lymph nodes, thyroid, salivary glands; red flags for head and neck cancer - persistent unexplained neck lump, hoarseness >3 weeks (smokers, over 45), non-healing mouth ulcer >3 weeks, red or red-and-white oral patches, unilateral ear pain with normal otoscopy (referred), dysphagia, unilateral nasal obstruction with bloody discharge (NICE NG12).
GALS Screening Examination
  • Gait, Arms, Legs, Spine - a rapid screen for musculoskeletal disease.
  • Three screening questions: Do you have any pain or stiffness in your muscles, joints or back? Can you dress yourself completely without difficulty? Can you walk up and down stairs without difficulty?
  • Gait - symmetry, smoothness, arm swing, stride length, ability to turn.
  • Spine - inspect from behind (scoliosis, muscle bulk), side (cervical lordosis, thoracic kyphosis, lumbar lordosis), and front; ear to shoulder (lateral cervical flexion), Schober's test (lumbar flexion - mark L5 and 10 cm above; increase <5 cm on bending suggests reduced flexion - ankylosing spondylitis), press over the midpoint of each supraspinatus (fibromyalgia tenderness).
  • Arms - hands behind head (shoulder abduction and external rotation), arms straight out (elbow extension), hands palms down then up (inspect for swelling, deformity, rashes, nail changes), squeeze the MCP joints (tenderness - inflammatory arthritis), make a fist (grip), pinch (fine precision), touch each finger to thumb.
  • Legs - inspect (quadriceps wasting, swelling, deformity), passive hip flexion and internal rotation (hip arthritis - first to be lost), knee crepitus and patellar tap (effusion), squeeze the MTP joints, inspect the soles (callosities - abnormal loading).
  • Record as a table of appearance and movement for gait, arms, legs and spine.
Regional Joint Examination
  • Look (skin - scars, erythema, psoriasis; swelling; deformity; muscle wasting; posture), feel (temperature with the back of the hand, tenderness, effusion, synovial thickening, crepitus), move (active then passive, range in degrees; pain; compare sides), special tests, function; examine the joint above and below; neurovascular status.
  • Hand - rheumatoid arthritis (ulnar deviation, swan neck and boutonnière deformities, Z-thumb, MCP and PIP swelling, rheumatoid nodules at the elbow, wasting, scars - joint replacement, tendon repair, carpal tunnel release); osteoarthritis (Heberden's nodes - DIP, Bouchard's nodes - PIP, squaring of the thumb base); psoriatic arthritis (DIP involvement, dactylitis, nail pitting, arthritis mutilans); gout (tophi); Dupuytren's; carpal tunnel tests (Tinel's - tap over the median nerve; Phalen's - wrist flexion for 60 seconds).
  • Shoulder - movements (flexion, extension, abduction, adduction, internal and external rotation); painful arc 60–120° (supraspinatus tendinopathy/impingement); loss of external rotation (adhesive capsulitis - frozen shoulder; glenohumeral arthritis); rotator cuff tests (empty can - supraspinatus; external rotation against resistance - infraspinatus/teres minor; lift-off or belly press - subscapularis); Hawkins–Kennedy and Neer's (impingement); apprehension test (instability).
  • Hip - gait (antalgic, Trendelenburg), Thomas' test (fixed flexion deformity), leg length (true - ASIS to medial malleolus; apparent - umbilicus to medial malleolus), range of movement (internal rotation lost first in OA), Trendelenburg test (stand on the affected leg - the pelvis drops on the opposite side if hip abductors are weak).
  • Knee - effusion (patellar tap, sweep test), quadriceps wasting, tenderness along joint lines (meniscal), range (flexion about 140°, full extension), ligaments - anterior and posterior drawer tests and Lachman's test (ACL), posterior sag (PCL), varus and valgus stress at 20–30° (collateral ligaments); McMurray's test (meniscal tears); patellar apprehension.
  • Ankle and foot - deformities (hallux valgus, pes planus/cavus, claw toes), Achilles tendon (Simmonds' (Thompson's) squeeze test - no plantar flexion when the calf is squeezed = rupture), Ottawa ankle rules for X-ray.
Back and Spine Examination
  • Look - posture, scoliosis (more visible on forward bending - rib hump), kyphosis, loss of lumbar lordosis (ankylosing spondylitis, muscle spasm), scars, skin (café-au-lait spots, hairy patch - spina bifida occulta).
  • Feel - spinous processes and paraspinal muscles for tenderness or step (spondylolisthesis), sacroiliac joints.
  • Move - cervical (flexion, extension, lateral flexion, rotation), thoracic rotation (seated), lumbar (flexion - Schober's, extension, lateral flexion).
  • Special tests - straight leg raise (L4–S1 root irritation - sciatic pain below the knee at 30–70°, worsened by ankle dorsiflexion - Bragard's/Lasègue), femoral nerve stretch test (prone, knee flexion - L2–4), crossed SLR (disc herniation).
  • Neurological examination of the lower limbs (myotomes, dermatomes, reflexes) and, if cauda equina is suspected, perianal sensation and anal tone.
  • Red flags for serious spinal pathology: age <20 or >50 at onset, history of cancer, unexplained weight loss, fever, immunosuppression, IV drug use, thoracic pain, night or constant pain, trauma (or minor trauma with osteoporosis), progressive neurological deficit, cauda equina features (bilateral sciatica, saddle anaesthesia, bladder or bowel dysfunction, sexual dysfunction) - emergency MRI.
At a Glance
FindingLesion
Spasticity, brisk reflexes, extensor plantarsUpper motor neuron
Wasting, fasciculations, absent reflexesLower motor neuron
Absent ankle jerks + extensor plantarsSACD, MND, Friedreich's, conus lesion
Dissociated "cape" sensory lossSyringomyelia
Forehead-sparing facial weaknessUMN (stroke)
Whole-face weaknessLMN (Bell's palsy)
Painful dilated pupil + ptosis + "down and out"Surgical third nerve palsy - aneurysm
Bitemporal hemianopiaChiasm (pituitary)
Weber lateralises to bad earConductive deafness
Positive RombergSensory (proprioceptive) ataxia
Painful arc 60–120°Supraspinatus impingement
Foot drop with preserved inversionCommon peroneal nerve palsy
Spot the Sign
  • Wasting of the thenar eminence and numbness of the thumb, index and middle fingers worse at night. → Carpal tunnel syndrome.
  • Fasciculating tongue, wasted hands and brisk reflexes with normal sensation. → Motor neuron disease.
  • Swan neck and boutonnière deformities with ulnar deviation. → Rheumatoid arthritis.
  • A young woman with headaches, obesity and bilateral swollen optic discs. → Idiopathic intracranial hypertension.
  • Unilateral hearing loss with Weber lateralising to the good ear and Rinne positive on both sides. → Sensorineural hearing loss - MRI for vestibular schwannoma.
  • Shuffling gait, urinary incontinence and cognitive decline. → Normal pressure hydrocephalus.
Exam-style Scenarios
  • Scenario. Present: increased tone in both legs, bilateral weakness of hip flexion and ankle dorsiflexion, brisk knee and ankle reflexes, extensor plantars, sensory level at T10, impaired vibration and proprioception.
    Answer: "This patient has a spastic paraparesis with a sensory level at T10, indicating a thoracic spinal cord lesion. Causes include compression (metastatic spinal cord compression, disc, abscess, haematoma), inflammatory myelitis (MS, NMO), B12 deficiency (though a sensory level suggests a structural lesion), and vascular causes. I would arrange an urgent whole-spine MRI, check bladder function and anal tone, and give dexamethasone if malignant cord compression is suspected."
  • Scenario. How do you distinguish a common peroneal nerve palsy from an L5 radiculopathy?
    Answer: Both cause foot drop and sensory loss over the dorsum of the foot. In L5 radiculopathy, ankle inversion (tibialis posterior - L5 via the tibial nerve) and hip abduction (gluteus medius) are also weak, and there is often back pain and a positive straight leg raise. In common peroneal palsy, inversion is preserved and there may be a history of compression at the fibular head (crossed legs, plaster cast, weight loss).
  • Scenario. An older patient presents with sudden painless loss of vision in one eye; the retina is pale with a cherry-red spot. What do you do?
    Answer: Central retinal artery occlusion - an ophthalmic and stroke emergency. Urgent same-day ophthalmology and stroke assessment; check ESR/CRP and ask about headache, jaw claudication and scalp tenderness (GCA - start high-dose steroids immediately if suspected); assess for embolic sources (carotid Doppler, ECG for AF, echo).
Key Points
  • Neurological examination: inspection, tone, power, reflexes, coordination, sensation - then localise.
  • Know myotomes, dermatomes and reflex roots.
  • Learn the cranial nerve sequence and key lesions (third nerve palsy, LMN versus UMN facial weakness, bulbar versus pseudobulbar palsy).
  • Fundoscopy: papilloedema, optic atrophy, diabetic and hypertensive retinopathy, CRAO and CRVO.
  • Joint examination: look, feel, move, special tests, function.
  • Know back pain red flags and cauda equina features.
Further Reading
  • Fuller G. Neurological Examination Made Easy
  • Macleod's Clinical Examination
  • Arthritis Research UK / Versus Arthritis: Clinical assessment of the musculoskeletal system - a handbook for medical students (GALS and REMS)
  • NICE NG59: Low back pain and sciatica in over 16s
  • NICE NG234: Spinal metastases and metastatic spinal cord compression
End of chapter 235