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Clinical science
Neurological examination
Summary
Neurological examination is the assessment of mental status, cranial nerves, motor function, sensory function,
coordination, and gait for the diagnosis of neurological conditions. Findings should always be compared with the
contralateral side and upper limb function should be compared to lower limb function to determine the location
of the lesion. This learning card provides information about several examination methods and explains a
selection of neurological terms used in the evaluation of neurological conditions.
Mutism: an inability or unwillingness to speak despite the faculties of speech being intact
Akinetic mutism: characterized by decreased motor responses and paucity of speech
Abulia: milder form of akinetic mutism that is characterized by disinterest and a slowed
mental state.
Orientation to person, place, and time
Mood and affect (as well as congruency)
Thought content (e.g., delusional) and process (e.g., logical thinking)
Memory (e.g., short-term vs. long-term memory, assessed by asking the patient to recall a number
of objects immediately and again after a few minutes)
Ability to perform simple calculations (e.g, simple multiplication; determine if appropriate for level
of education)
Insight and judgement (ask patient what they would do in a realistic situation, e.g., if they found a
stamped envelope)
Higher cortical function (e.g., ask patients to explain the meaning of well-known idioms)
Determine levels of consciousness
Mini-mental status examination (MMSE)
Saint Louis University Mental Status Examination (SLUMS)
Findings
Hemineglect
Inability to respond to unilateral stimuli due to a brain lesion (not due to a primary motor or sensory
lesion)
The lesion is usually contralateral to the stimuli
Motor neglect
Sensory or perceptual neglect
Amnesia: loss of memory (e.g., time, content)
Retrograde amnesia: loss of memory-access to events that occurred and/or information acquired
prior to the incident
Anterograde amnesia: loss of memory-access to events that occurred and/or information acquired
after the incident
Global amnesia: loss of memory-access to events that occurred and/or information acquired prior
and after the incident
Aphasia: Inability to communicate (impairment of the ability to either form or understand language)
Telegraphic and
grammatically incorrect
nonfluent speech
Broca aphasia (motor Comprehension is largely
aphasia, expressive Broca area (frontal lobe) spared (difficulty
aphasia) understanding complex
language may occur)
The patient is typically aware
of the deficits
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Apraxia: difficulty performing targeted, voluntary movements despite intact motor function
Ideomotor apraxia: difficulty imitating actions; intended expression and gestures do not match
Ideational apraxia: difficulty completing multistep actions.
Visual motor apraxia: difficulty picking up objects placed in the contralesional visual field.
Agnosia: Impairment of recognition of sensory stimulus (most commonly visual) [1]
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Tactile agnosia (astereognosis): Impaired ability to recognize or identify objects by touch alone;
visual recognition is unimpaired.
Visuospatial dysgnosia: inability to orient oneself in space
Prosopagnosia: inability to recognize familiar faces
Autotopagnosia
Anosognosia: inability to recognize one's own neurologic impairment
Alexia: form of visual agnosia with severe reading problems, as a result of interrupted connections
between the visual cortex and language‑related areas. Subtypes include pure alexia without agraphia,
alexia with agraphia, and aphasic alexia.
Acalculia: inability to perform simple calculations (parietal lobe lesion)
Agraphia: inability to write
References:[2][3][4]
Optic nerve II
The examiner shines a light into the patient's eye (e.g.,
a penlight).
A prompt, consensual response should normally be
Pupillary light reflex observable.
Pupillary shape and width: Healthy pupils are isocoric
and of medium width; anisocoric and/or narrow/wide
are suggestive of a disorder (see pupillary disorders).
Oculomotor III,
nerve, trochlear IV, Patients are asked to follow a finger moving up, down,
nerve, abducens VI Eye movement laterally, and diagonally with their eyes.
nerve Observe if there is paresis, alterations in smooth
pursuit appear, or nystagmus,
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Muscle function The patient is asked to open and close his/her mouth;
(muscles of at the same time, the examiner palpates the masseter
mastication) muscle.
Trigeminal nerve V
Masseter reflex (jaw jerk reflex)
A finger is placed on the patient's chin, while
the patient's mouth remains slightly open
Tapping with a reflex hammer normally induces
jaw closure
If jaw closure is increased, suspect an UMN
Reflexes
lesion
Corneal reflex
The cornea is lightly touched with a cotton
swab (approaching slowly and sideways from
the lid edge)
Touch normally induces closing of the eyelid.
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X only (recurrent
In case of lesion, the patient would have hoarseness or
laryngeal nerve):
bovine cough.
vocalization
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References:[3]
Motor function
Upper motor neuron (UMN) injury vs. lower motor neuron (LMN) injury
Lower motor neuron lesion (LMN
Upper motor neuron lesion (UMN damage)
damage)
Muscle Atrophied
Atrophy is absent
appearance Fasciculations
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Upper motor neuron (UMN) injury vs. lower motor neuron (LMN) injury
Lower motor neuron lesion (LMN
Upper motor neuron lesion (UMN damage)
damage)
Muscle appearance
Assessment: inspection and palpation of muscle groups
Findings
Fasciculation: involuntary, asynchronous contraction of muscle fascicles within a single motor unit;
usually benign but can signify a lower motor neuron lesion
Tenderness
Abnormal movements (e.g., tremor, tic, myoclonus)
Abnormal posture
Atrophy or hypertrophy (examined bilaterally)
Muscle groups are measured to compare specific differences in size.
In neurologic disorders, the small hand muscles are often affected by atrophy.
References:[3]
Power
Definition: maximal effort a patient is able to exert from an individual muscle or group of muscles
Assessment
The patient is asked to flex and extend extremities against resistance
Muscle power tests should be performed bilaterally for comparison
Muscle power grading
0 = no contraction (paresis)
1 = flicker or trace of contraction
2 = active movement, with gravity eliminated
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References:[5]
Reflexes
Tendon reflexes
Definition: stretch, monosynaptic reflexes
Assessment
During reflex testing, the patient should be relaxed (at least the muscles involved in the reflex test
should be relaxed). (→ also see: radiculopathy)
Elderly patients may have reduced or absent lower deep tendon reflexes due to normal aging-related
changes in muscles and tendons
A reflex to test the integrity of a sensory and motor neuron circuit
Upon tapping of the reflex hammer, activation of the dorsal root ganglion causes firing of the
lower motor neuron for the agonist muscle and relaxation of the antagonist muscle, resulting
in automatic movement.
An increased DTR indicates an upper motor neuron issue, whereas decreased DTR indicates a
LMN, neuromuscular junction, or muscle issue.
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Superficial reflexes
Definition: polysynaptic reflexes elicited by stimulation of the skin
Superficial reflexes are divided into two subgroups:
Physiological reflexes
Pathological superficial reflexes: in case of central motor neuron damage, the reflex response
decreases.
Nerve
Reflex Test
root
Abdominal reflexes are tested with the patient lying down. The anterior abdominal
wall is lightly stroked with a spatula from lateral to medial (bilaterally) in following
areas:
The reflex is elicited by stroking the medial, inner part of the thigh. A normal response
L1– Cremasteric
is a contraction of the cremaster muscle that pulls up the testis on the same side of the
L2 reflex
body.
Stroking the skin around the anus with a spatula elicits the anal reflex, which results in
Anal reflex
S3– a contraction of the anal sphincter muscles.
S5
Bulbocavernosus The reflex is elicited by squeezing the glans penis or clitoris, resulting in contractions
reflex of the pelvic floor muscles.
Primitive reflexes
Brief description: Reflexes that are are normal in newborns and infants, but not in adults, where they may
appear in case of diffuse brain injury due to lack of common inhibiting factors
Test
Sucking reflex Stroking the mouth induces sucking activity.
Palmar grasp
Stroking the palms elicits finger flexion.
reflex
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Test
Palmomental Stroking the ipsilateral thenar eminence from proximal to distal induces a short involuntary
reflex contraction of the mentalis muscle.
Brief description
Corticospinal tract signs are indicative of damage to the pyramidal tract.
Babinski sign is the most common and thus most reliable pyramidal tract sign.
These reflexes occur physiologically in healthy infants
Test Sign
The examiner strokes the sole of a
Babinski
patient's foot on the lateral edge using, The sign is positive (pathological) when the big toe extends
sign
e.g., the handle of a reflex hammer (dorsiflexes), while the other toes fan out. The test is
Gordon The examiner compresses the calf inconclusive when only the big toe responds.
sign muscles
Babinski sign, although normal in newborns and infants, is always pathological in adults!
Do not confuse clonus with myoclonus! Myoclonus is arrhythmical and defined by sudden jerks of a muscle or
group of muscles while clonus is rather rhythmic and defined by repetitive contractions and relaxations of a
muscle group!
Tone
Definition: resistance of an individual muscle (or a group of muscles) to passive stretching
Assessment: passive movement of the extremities
Tests
Upper limb Lower limb
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Tests
Upper limb Lower limb
Velocity-dependent phenomenon
The clasp-knife phenomenon: initial The arm of the examiner is placed under the
Spasticity resistance due to increased muscle tone patient's knee and the examiner briskly lifts the
is followed by a sudden decrease in patient's limb → increased muscle tone in limb
resistance.
Velocity-independent phenomenon
Cogwheel rigidity: A resistance
Stiffness and/or inflexibility regardless of
Rigidity resembling a cogwheel movement is
movement
observed when the joint of a patient's
extremity is moved by the examiner.
Sensation
Pathway Assessment Finding
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Abnormalities of
A tuning fork is hit and placed on a bony vibration are described
projection (e.g., medial malleolus). as mild, moderate, or
Pallesthesia The vibration amplitude and thus severe loss of vibration
Dorsal
(vibration the vibration intensity decrease sense (pallhypesthesia).
columns
sense) over time. Loss of vibration sense
The patient reports when the may also indicate a
vibration stops. peripheral neuropathy or
myelopathy.
References:[3][6]
Coordination
Definition: ability to coordinate fluid movements
Assessment
Finger-to-nose test
Heel-knee-shin test
Rapid alternating movement test
Findings
Dysmetria
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Dysdiadochokinesia
See also cerebellar syndromes.
References:[3]
Gait assessment
Evidence for vestibular disorders, sensory or cerebellar ataxia (see “Diagnostics” in cerebellar syndromes)
Assessment
Observation of casual gait: The patient is asked to walk a few steps forwards and backwards.
Normal gait: steady, natural arm swing
Abnormal gait: broad-based or unsteady gait, short-stepping gait
Balance test: The patient is asked to place one foot directly in front of the other as if walking on a
tightrope
Foot drop test: The patient is asked to walk on their heels (impossible in the case of deep fibular
nerve lesions)
Walking on tiptoes (impossible in the case of tibial nerve lesions)
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