Nervous system
History & Examination
Cardinal symptoms
 Altered sensorium
 Seizures
 Weakness
 Paresthesias
 Loss of function
 Abnormal movements
 Headache
 Abnormal behaviour
Nervous system
 Brain
 Cerebrum
 Midbrain
 Pons/medulla
 Cerebellum
 Cranial nerves- I-XII
 Spinal cord
 Peripheral nerves
Nervous system examination
 Consciousness
 Higher mental function
 Cranial nerves
 Motor system
 Sensory system
 Coordination
 Gait
 Meningial irritation, Skull, Spine
Consciousness
 Includes level (wakefulness) & content (awareness)
 Controlled by cerebral hemispheres & RAS in
brainstem
 Levels-
 Drowsy- arousable with verbal stimuli
 Stupor- arousable with painful stimuli
 Coma- not arousable
 Content-
 Confusion- a state of inattention & lack of clarity in thinking
(incoherent)
 Glasgow Coma Scale (GCS)- Eye.Motor.Vocal
Released reflexes
 In demented & confused patient
 Grasping- stroking of radial surface of palm, asso.
with C/L frontal lobe lesion
 Avoiding- stroking of ulnar surface of palm, asso. with
C/L parietal lobe lesion
 Glabellar tap
 Snout
 Sucking
Higher mental functions
 Orientation- time, place, person
 Memory- immediate, recent, remote
 Attention
 Calculation
 Language
Language
 Components-
 Articulation- Dysarthria
 Fluency
 Naming
 Repetition }Dysphasia
 Comprehension
 Reading
 Writing
Apraxia, Agnosia, Aphasia
 Apraxia- loss of ability to carry out learned
purposeful movements
 Agnosia- loss of ability to recognise, with
intact sensations & memory
 Aphasia- impairment of structure &
organization of language
 Receptive (fluent)- Wernicke’s
 Expressive (nonfluent)- Broca’s
 Dysarthria- defect in articulation &
enunciation of speech
Cranial nerves
 I- olfactory- sensory, smell
 II- optic- visual acuity/field, color vision
 III- oculomotor- MR,SR,IR,IO muscles,
sphincter pupillae (accomodation), levator
palpebrae superioris
 IV- trochlear- motor, superior oblique (SO4)
 VI- abducent- motor, lateral rectus (LR6)
AbR.OAd- abducted recti, obliques adducted
III, IV, VI nerve defect
 Squint/strabismus (paralytic)- secondary
(normal eye) > primary (affected eye)
deviation
 Diplopia- double image- true distinct &
false indistinct/blurred
 Head tilt- in the direction of affected muscle
 Past pointing- to same side on looking with
the affected eye
 Loss of accomodation
 Ptosis
Cranial nerves
 V- trigeminal- sensory to face
(cornea), motor to muscles of
mastication, controls oral secretion
 VII- facial- motor to all scalp & facial
muscles of expression except LPS,
taste sensation in ant. 2/3rd
of tongue
Facial palsy
 Supranuclear
 Lower face affected
 Emotional response
may be affected
 Taste intact
 Facial reflexes
increased
 No atrophy
 Infranuclear
 Whole face affected
 Emotional response
& reflexes affected
 Taste affected
 Hyperacusis
 Corneal reflex -nt
 Atrophy
Cranial nerves
 VIII- vestibulocochlear- balance & hearing-
vertigo, nystagmus, tinnitus, impaired
hearing, caloric tests, Rinne/Weber test
 IX- glossopharyngeal- sensory to post. 1/3rd
of tongue & pharynx
 X- vagus- motor to palate & pharynx
 XI- accessory- motor to sternomastoid &
trapezius
 XII- hypoglossal- motor to tongue
Motor system
 Upper motor neurons-
Corticospinal fibers from Frontal motor cortex 
Internal capsule  Pyramids in medulla 
crossover  Lateral corticospinal tract
(UM,LL)  terminates in anterior horn
 Lower motor neurons-
Anterior horn cells  Anterior spinal nerve root
 Peripheral nerve
Lesion
 Upper motor neuron
 Weakness
 Disuse atrophy
 Spasticity
 Reflexes
 Extensor plantar
 NCV- normal
 No denervation
potentials in EMG
 Lower motor neuron
 Pronounced weakness
 Wasting
 Flaccidity
 Loss of reflexes
 Fasciculations
 NCV- abnormal
 Denervation potentials
in EMG
Motor system examination
 Bulk
 Tone
 Power
 Reflexes
 Coordination
 Gait
 Involuntary movement
Power- grading
 0- complete paralysis
 1- flicker (any slightest movement)
 2- movement with gravity excluded
 3- movement against gravity but
not against resistance
 4- mild weakness
 5- normal power
Deep tendon reflexes (DTR)
 Jaw jerk- lesion
above trigeminal
motor nucleus-pons
 Supinator- C 5/6
 Biceps- C 5/6
 Triceps- C 6/7
 Knee- L 2-4
 Ankle- S 1/2
 Grading
 0- absent
 1- present
 2- brisk
 3- very brisk
 4- clonus
Superficial reflexes
 Corneal- trigeminal or facial nerve
 Palatal- IX-X cranial nerves
 Scapular- C5-T1
 Abdominal- T7-12
 Cremasteric- L1/2
 Plantar- L5/S1- extensor always abnormal
except age <1 year & postictal
 Bulbocavernosus- S3/4
 Anal- S3/4
Plantar reflex
 L5/S1
 Normally flexion of toes
 Extensor plantar reflex- components
 Extension of big toe, fanning of other toes, dorsiflexion of ankle,
flexion of knee, flexion of hip
 How to elicit?
 Babinski- stroke plantar surface of foot laterally from heel to toe
 Chaddock- stroke dorsal surface of foot laterally
 Oppenheim- stroke shin downwards
 Gordon- pinch/squeeze calf muscles
 Shaeffer- pinch Achilles tendon
 Extensor response denotes UMN lesion
Spinal segment & vertebra
 Vertebral column is longer than spinal cord
 Vertebra & corresponding spinal cord
segment
 Cervical vertebrae- +1
 Thoracic 1-6- +2
 Thoracic 7-9- +3
 T10- L1 & L2
 T11- L3 & L4
 T12- L5
 L1- sacral segments
Coordination
 Needs sensory input (joint/position),
cerebellum (lobes) & muscle tone
 Tests-
 Finger-nose test
 Rapid finger movements (touching the thumb)
 Dysdiadochokinesia
 Heel-shin test
 Walking in straight line  Tandem walking
 Romberg’s sign
Gait
 Legs exposed, feet bare
 Abnormal gait-
 Spastic- narrow base, knees extended, feet drag, circumduction
 Sensory ataxic- stamping with heel first
 Cerebellar ataxic- broad base, ‘drunken’
 Festinant (parkinsonian)- rapid, short shuffling steps
 Waddling (myopathic)- body tilted backwards, feet wide apart,
body sways sideways with each step
 High-stepping (peripheral neuropathic)- high step, toes landing
first
Involuntary movements
 Mostly due to disease of basal ganglia &
extrapyramidal system
 Types-
 Myoclonus- rapid irregular jerks of a group of muscles
 Tremor- distal, oscillatory, resting (P)/intentional (C)
 Athetosis- distal writhing purposeless movement
 Chorea- arrythmic forcible, jerky, rapid, restless movements
 Dystonia- abnormally maintained posture, plastic rigidity
 Hemiballismus- involuntary rapid violent flailing of arm
 Tics- repetitive abnormal movements, embarassing
Sensory system
 Receptors in skin  Peripheral nerves 
Posterior roots  Spinal cord (post. horn)
 Pain/temp./crude touch fibers crossover & ascend
in anterolateral spinothalamic tracts (UM,LL)
 Fine touch/position/vibration fibers ascend
ipsilaterally in posterior columns (LM,UL) that
crossover in medulla & travel in medial lemniscus
 Both join in thalamus, from where sensory
fibers travel via internal capsule to Parietal
cortex
Testing sensations
 From abnormal to normal areas
 Mark boundaries/dermatomes
 Touch & 2-point discrimination
 Vibration- tested at bony prominences
 Position- <10 degree movement can be appreciated
at all joints
 Pain- superficial (pin prick) & deep (muscle squeeze)
 Temperature
 Recognition of size/shape/weight/form
Other tests
 Meningeal irritation- neck rigidity,
Kernig’s sign (extend knee with hip
flexed)
 Straight leg raising test
 Deformity of skull or spine
Abbreviated neuro. exam.
 Pupils & ocular movements & fundus
 Facial movements
 Speech
 Power in arms & legs
 DTR & plantar reflex
 Pain & vibration in hands & feet
 Gait
Supported by
LP, X-ray, EMG/NCV, CT & MRI

Nervous system exam

  • 1.
  • 2.
    Cardinal symptoms  Alteredsensorium  Seizures  Weakness  Paresthesias  Loss of function  Abnormal movements  Headache  Abnormal behaviour
  • 3.
    Nervous system  Brain Cerebrum  Midbrain  Pons/medulla  Cerebellum  Cranial nerves- I-XII  Spinal cord  Peripheral nerves
  • 4.
    Nervous system examination Consciousness  Higher mental function  Cranial nerves  Motor system  Sensory system  Coordination  Gait  Meningial irritation, Skull, Spine
  • 5.
    Consciousness  Includes level(wakefulness) & content (awareness)  Controlled by cerebral hemispheres & RAS in brainstem  Levels-  Drowsy- arousable with verbal stimuli  Stupor- arousable with painful stimuli  Coma- not arousable  Content-  Confusion- a state of inattention & lack of clarity in thinking (incoherent)  Glasgow Coma Scale (GCS)- Eye.Motor.Vocal
  • 6.
    Released reflexes  Indemented & confused patient  Grasping- stroking of radial surface of palm, asso. with C/L frontal lobe lesion  Avoiding- stroking of ulnar surface of palm, asso. with C/L parietal lobe lesion  Glabellar tap  Snout  Sucking
  • 7.
    Higher mental functions Orientation- time, place, person  Memory- immediate, recent, remote  Attention  Calculation  Language
  • 8.
    Language  Components-  Articulation-Dysarthria  Fluency  Naming  Repetition }Dysphasia  Comprehension  Reading  Writing
  • 9.
    Apraxia, Agnosia, Aphasia Apraxia- loss of ability to carry out learned purposeful movements  Agnosia- loss of ability to recognise, with intact sensations & memory  Aphasia- impairment of structure & organization of language  Receptive (fluent)- Wernicke’s  Expressive (nonfluent)- Broca’s  Dysarthria- defect in articulation & enunciation of speech
  • 10.
    Cranial nerves  I-olfactory- sensory, smell  II- optic- visual acuity/field, color vision  III- oculomotor- MR,SR,IR,IO muscles, sphincter pupillae (accomodation), levator palpebrae superioris  IV- trochlear- motor, superior oblique (SO4)  VI- abducent- motor, lateral rectus (LR6) AbR.OAd- abducted recti, obliques adducted
  • 11.
    III, IV, VInerve defect  Squint/strabismus (paralytic)- secondary (normal eye) > primary (affected eye) deviation  Diplopia- double image- true distinct & false indistinct/blurred  Head tilt- in the direction of affected muscle  Past pointing- to same side on looking with the affected eye  Loss of accomodation  Ptosis
  • 12.
    Cranial nerves  V-trigeminal- sensory to face (cornea), motor to muscles of mastication, controls oral secretion  VII- facial- motor to all scalp & facial muscles of expression except LPS, taste sensation in ant. 2/3rd of tongue
  • 13.
    Facial palsy  Supranuclear Lower face affected  Emotional response may be affected  Taste intact  Facial reflexes increased  No atrophy  Infranuclear  Whole face affected  Emotional response & reflexes affected  Taste affected  Hyperacusis  Corneal reflex -nt  Atrophy
  • 14.
    Cranial nerves  VIII-vestibulocochlear- balance & hearing- vertigo, nystagmus, tinnitus, impaired hearing, caloric tests, Rinne/Weber test  IX- glossopharyngeal- sensory to post. 1/3rd of tongue & pharynx  X- vagus- motor to palate & pharynx  XI- accessory- motor to sternomastoid & trapezius  XII- hypoglossal- motor to tongue
  • 15.
    Motor system  Uppermotor neurons- Corticospinal fibers from Frontal motor cortex  Internal capsule  Pyramids in medulla  crossover  Lateral corticospinal tract (UM,LL)  terminates in anterior horn  Lower motor neurons- Anterior horn cells  Anterior spinal nerve root  Peripheral nerve
  • 16.
    Lesion  Upper motorneuron  Weakness  Disuse atrophy  Spasticity  Reflexes  Extensor plantar  NCV- normal  No denervation potentials in EMG  Lower motor neuron  Pronounced weakness  Wasting  Flaccidity  Loss of reflexes  Fasciculations  NCV- abnormal  Denervation potentials in EMG
  • 17.
    Motor system examination Bulk  Tone  Power  Reflexes  Coordination  Gait  Involuntary movement
  • 18.
    Power- grading  0-complete paralysis  1- flicker (any slightest movement)  2- movement with gravity excluded  3- movement against gravity but not against resistance  4- mild weakness  5- normal power
  • 19.
    Deep tendon reflexes(DTR)  Jaw jerk- lesion above trigeminal motor nucleus-pons  Supinator- C 5/6  Biceps- C 5/6  Triceps- C 6/7  Knee- L 2-4  Ankle- S 1/2  Grading  0- absent  1- present  2- brisk  3- very brisk  4- clonus
  • 20.
    Superficial reflexes  Corneal-trigeminal or facial nerve  Palatal- IX-X cranial nerves  Scapular- C5-T1  Abdominal- T7-12  Cremasteric- L1/2  Plantar- L5/S1- extensor always abnormal except age <1 year & postictal  Bulbocavernosus- S3/4  Anal- S3/4
  • 21.
    Plantar reflex  L5/S1 Normally flexion of toes  Extensor plantar reflex- components  Extension of big toe, fanning of other toes, dorsiflexion of ankle, flexion of knee, flexion of hip  How to elicit?  Babinski- stroke plantar surface of foot laterally from heel to toe  Chaddock- stroke dorsal surface of foot laterally  Oppenheim- stroke shin downwards  Gordon- pinch/squeeze calf muscles  Shaeffer- pinch Achilles tendon  Extensor response denotes UMN lesion
  • 22.
    Spinal segment &vertebra  Vertebral column is longer than spinal cord  Vertebra & corresponding spinal cord segment  Cervical vertebrae- +1  Thoracic 1-6- +2  Thoracic 7-9- +3  T10- L1 & L2  T11- L3 & L4  T12- L5  L1- sacral segments
  • 23.
    Coordination  Needs sensoryinput (joint/position), cerebellum (lobes) & muscle tone  Tests-  Finger-nose test  Rapid finger movements (touching the thumb)  Dysdiadochokinesia  Heel-shin test  Walking in straight line  Tandem walking  Romberg’s sign
  • 24.
    Gait  Legs exposed,feet bare  Abnormal gait-  Spastic- narrow base, knees extended, feet drag, circumduction  Sensory ataxic- stamping with heel first  Cerebellar ataxic- broad base, ‘drunken’  Festinant (parkinsonian)- rapid, short shuffling steps  Waddling (myopathic)- body tilted backwards, feet wide apart, body sways sideways with each step  High-stepping (peripheral neuropathic)- high step, toes landing first
  • 25.
    Involuntary movements  Mostlydue to disease of basal ganglia & extrapyramidal system  Types-  Myoclonus- rapid irregular jerks of a group of muscles  Tremor- distal, oscillatory, resting (P)/intentional (C)  Athetosis- distal writhing purposeless movement  Chorea- arrythmic forcible, jerky, rapid, restless movements  Dystonia- abnormally maintained posture, plastic rigidity  Hemiballismus- involuntary rapid violent flailing of arm  Tics- repetitive abnormal movements, embarassing
  • 26.
    Sensory system  Receptorsin skin  Peripheral nerves  Posterior roots  Spinal cord (post. horn)  Pain/temp./crude touch fibers crossover & ascend in anterolateral spinothalamic tracts (UM,LL)  Fine touch/position/vibration fibers ascend ipsilaterally in posterior columns (LM,UL) that crossover in medulla & travel in medial lemniscus  Both join in thalamus, from where sensory fibers travel via internal capsule to Parietal cortex
  • 27.
    Testing sensations  Fromabnormal to normal areas  Mark boundaries/dermatomes  Touch & 2-point discrimination  Vibration- tested at bony prominences  Position- <10 degree movement can be appreciated at all joints  Pain- superficial (pin prick) & deep (muscle squeeze)  Temperature  Recognition of size/shape/weight/form
  • 28.
    Other tests  Meningealirritation- neck rigidity, Kernig’s sign (extend knee with hip flexed)  Straight leg raising test  Deformity of skull or spine
  • 29.
    Abbreviated neuro. exam. Pupils & ocular movements & fundus  Facial movements  Speech  Power in arms & legs  DTR & plantar reflex  Pain & vibration in hands & feet  Gait
  • 30.
    Supported by LP, X-ray,EMG/NCV, CT & MRI