1. THE NEUROLOGICAL EXAMINATION
Prof Mohammad Abduljabbar

2. Resources Neuroanatomy through Clinical Cases by Hal Blumenfeld
The Technique of the Neurologic Examination by William DeMyer
DeJong’s Neurologic Examination by William W. Campbell

3. You must do a minimum basic examination on every patient but you don’t need to do every test

4. Tools of the trade

5. NEUROLOGICAL EXAM MENTAL STATUS CRANIAL NERVES MOTOR EXAM REFLEXES
STRENGTH
GAIT
CEREBELLAR
REFLEXES
SENSATION

6. MENTAL STATUS

7. Level of Consciousness
Awake and alert
Agitated
Lethargic
Arousable with
Voice
Gentle stimulation
Painful/vigorous stimulation
Comatose

8. Mental Status Exam 1. Level of alertness,attention and cooperation
We can test attention by seeing if the patient can remain focused on a simple task, such as spelling a short word forward and backward (W-O-R-L-D / D-L-R-O-W is a standard), repeating a string of integers forward and backward (digit span), or naming the months forward and then backward. Normal digit span is 6 or more forward, and 4 or more backward, depending slightly on age and education. Degree of cooperation should be noted, especially if it is abnormal, since this will influence many aspects of the exam.

9. LANGUAGE FLUENCY NAMING REPETITION READING WRITING COMPREHENSION
Aphasia vs. dysarthria

10. Mental Status Exam 3. Speech and language
Spontaneous speech: Note the patient's fluency, including phrase length, rate, and abundance of spontaneous speech. Also note tonal modulation and whether paraphasic errors (inappropriately substituted words or syllables), neologisms (nonexistent words), or errors in grammar are present.
Comprehension: Can the patient understand simple questions and commands? Comprehension of grammatical structure should be tested as well
Naming: Ask the patient to name some easy (pen, watch, tie, etc.) and some more difficult (fingernail, belt buckle, stethoscope, etc.) objects
Repetition: Can the patient repeat single words and sentences (a standard is "no ifs ands or buts")?
Reading: Ask the patient to read single words, a brief passage, and the front page of the newspaper aloud and test for comprehension.
Writing: Ask the patient to write their name and write a sentence.

11. MEMORY IMMEDIATE REMOTE 3 OBJECTS AT 0/3/5 MINUTES HISTORICAL EVENTS
REALLY A MEASURE OF ATTENTION RATHER THAN MEMORY
REMOTE
3 OBJECTS AT 0/3/5 MINUTES
HISTORICAL EVENTS
PERSONAL EVENTS

12. Mental Status Exam 4. Memory for recent and remote events
Recent memory: Ask the patient to recall three items or a brief story after a delay of 3 to 5 minutes. Be sure the information has been registered by asking the patient to repeat it immediately before initiating the delay. Provide distracters during the delay to prevent the patient from rehearsing the items repeatedly.
Remote memory: Ask the patient about historical or verifiable personal events.
Memory can be impaired on many different timescales. Impaired ability to register and recall something within a few seconds after it was said is an abnormality that blends into the category of impaired attention. If immediate recall is intact, then difficulty with recall after about 1 to 5 minutes usually signifies damage to the limbic memory structures located in the medial temporal lobes and medial diencephalon

13. ORIENTATION
PERSON
NOT WHO THEY ARE BUT WHO YOU ARE
PLACE
TIME

14. OTHER COGNITIVE FUNCTIONS
CALCULATION
ABSTRACTION
SIMILARITIES/DIFFERENCES
JUDGEMENT
PERSONALITY/BEHAVIOR

15. Mental Status Exam 6. Apraxia
The term apraxia will be used here to mean inability to follow a motor command that is not due to a primary motor deficit or a language impairment. It is apparently caused by a deficit in higher-order planning or conceptualization of the motor task. You can test for apraxia by asking the patient to do complex tasks, using commands such as "Pretend to comb your hair" or "Pretend to strike a match and blow it out" and so on. Patients with apraxia perform awkward movements that only minimally resemble those requested, despite having intact comprehension and an otherwise normal motor exam. This kind of apraxia is sometimes called ideomotor apraxia. In some patients, rather than affecting the distal extremities, apraxia can involve primarily the mouth and face, or movements of the whole body, such as walking or turning around.

16. Mental Status Exam Folstein Mini-mental status exam
This is a screening tool used to follow the cognitive decline associated with dementia. It has been in wide use since 1975 and takes 5-10 minutes to administer. It is a limited test instrument. This examination is not suitable for making a diagnosis but can be used to indicate the presence of cognitive impairment, such as when dementia or head injury are suspected. People from different cultural groups or low intelligence or education may score poorly on this examination in the absence of cognitive impairment and well educated people may score well despite having cognitive impairment

17. Mental Status Exam 9. Sequencing tasks and frontal release signs
Frontal lobe lesions in adults can cause the reemergence of certain primitive reflexes that are normally present in infants. These so-called frontal release signs include the grasp, snout, root, and suck reflexes. Of these reflexes, the grasp reflex is the most useful in evaluating frontal lobe dysfunction.
Patients with frontal lobe dysfunction may have particular difficulty in changing from one action to the next when asked to perform a repeated sequence of actions.This phenomenon is called perseveration

18. Mental Status Exam 10. Delusions and Hallucinations
Does the patient have any delusional thought processes? Does he have auditory or visual hallucinations? Ask questions such as, "Do you ever hear things that other people don't hear or see things that other people don't see?" "Do you feel that someone is watching you or trying to hurt you?" "Do you have any special abilities or powers?"
These abnormalities can be seen in toxic or metabolic abnormalities and other causes of diffuse brain dysfunction, and in primary psychiatric disorders. In addition, abnormal sensory phenomena can be caused by focal lesions or seizures in visual, somatosensory, or auditory cortex, and thought disorders can be caused by lesions in the association cortex and limbic system

19. Mental Status Exam 11. Mood
Signs of major depression include depressed mood, changes in eating and sleeping patterns, loss of energy and initiative, low self-esteem, poor concentration, lack of enjoyment of previously pleasurable activities, and self-destructive or suicidal thoughts and behavior. Anxiety disorders are characterized by preoccupation with worrisome thoughts. Mania causes patients to be abnormally active and cognitively disorganized.

20. CRANIAL NERVES

21. CRANIAL NERVE EXAM I - OLFACTORY II - OPTIC
DON’T USE A NOXIOUS STIMULUS
COFFEE, LEMON EXTRACT
II - OPTIC
VISUAL ACUITY
VISUAL FIELDS
FUNDOSCOPIC EXAM

22. Cranial Nerve1 Olfaction
Not tested much unless a frontal lobe tumor is suspected
May be damaged in patients with closed head injuries,nasal obstruction,viral infections, and can be abnormal in Parkinsons disease, Alzheimer’s,and Multiple Sclerosis
Test by asking if patients can smell,coffee,vanilla, or cinnamon in each nostril. Avoid noxious odors ( ie NH3)

24. Cranial Nerve 2 Optic Nerve
Visual Acuity (test with hand card)
Color Vision (loss of color vision especially red is an important symptom of optic neuritis)
Visual Fields (can be tested at the bedside by counting fingers in each quadrant)
Visual Extinction (to detect visual neglect)
Funduscopic Examination

26. Cranial Nerve 2 and 3 Pupillary responses
The size and shape of the pupil should be recorded at rest. Under normal conditions, the pupil constricts in response to light. Note the direct response, meaning constriction of the illuminated pupil, as well as the consensual response, meaning constriction of the opposite pupil.
Test the pupillary response to accommodation. Normally, the pupils constrict while fixating on an object being moved from far away to near the eyes.
Direct response (pupil illuminated). The direct response is impaired in lesions of the ipsilateral optic nerve, the pretectal area, the ipsilateral parasympathetics traveling in CN III, or the pupillary constrictor muscle of the iris.
Consensual response (contralateral pupil illuminated). The consensual response is impaired in lesions of the contralateral optic nerve, the pretectal area, the ipsilateral parasympathetics traveling in CN III, or the pupillary constrictor muscle.
Accommodation (response to looking at something moving toward the eye). Accommodation is impaired in lesions of the ipsilateral optic nerve, the ipsilateral parasympathetics traveling in CN III, or the pupillary constrictor muscle, or in bilateral lesions of the pathways from the optic tracts to the visual cortex. Accommodation is spared in lesions of the pretectal area.

27. Pupillary Size is determined by the light input, sympathetic and parasympathetic tone
Text

28. CRANIAL NERVE EXAM III/IV/VI OCULMOTOR, TROCHLEAR, ABDUCENS
PUPILLARY RESPONSE
EYE MOVEMENTS
OBSERVE LIDS FOR PTOSIS
V - TRIGEMINAL
MOTOR - JAW STRENGTH
SENS - ALL 3 DIVISIONS

29. Cranial Nerve 3,4,6 Extraocular Movements
Observe the eyes at rest to see if there are any abnormalities such as spontaneous nystagmus (see below)or dysconjugate gaze (eyes not both fixated on the same point) resulting in diplopia (double vision)
Test smooth pursuit by having the patient follow an object moved across their full range of horizontal and vertical eye movements. Test convergence movements by having the patient fixate on an object as it is moved slowly towards a point right between the patient's eyes
In comatose or severely lethargic patients, the vestibulo-ocular reflex can be used to test whether brainstem eye movement pathways are intact. The oculocephalic reflex, a form of the vestibulo-ocular reflex, is tested by holding the eyes open and rotating the head from side to side or up and down

30. Cranial Nerve 5 Facial Sensation and Muscles of Mastication
Test facial sensation using a cotton wisp and a sharp object. Also test for tactile extinction using double simultaneous stimulation.
The corneal reflex, which involves both CN 5 and CN 7, is tested by touching each cornea gently with a cotton wisp and observing any asymmetries in the blink response.
Feel the masseter muscles during jaw clench. Test for a jaw jerk reflex by gently tapping on the jaw with the mouth slightly open.

32. CRANIAL NERVES VII - FACIAL VIII - VESTIBULAR
OBSERVE FOR FACIAL ASYMMETRY
FOREHEAD WRINKLING, EYELID CLOSURE, WHISTLE/PUCKER
VIII - VESTIBULAR
ACUITY
RINNE, WEBER

33. Cranial Nerve 7 Muscles of Facial Expression and Taste
Look for asymmetry in facial shape or in depth of furrows such as the nasolabial fold. Also look for asymmetries in spontaneous facial expressions and blinking. Ask patient to smile, puff out their cheeks, clench their eyes tight, wrinkle their brow, and so on. Old photographs of the patient can often aid your recognition of subtle changes
Check taste with sugar, salt, or lemon juice on cotton swabs applied to the lateral aspect of each side of the tongue. Like olfaction, taste is often tested only when specific pathology is suspected, such as in lesions of the facial nerve, or in lesions of the gustatory nucleus
The upper motor neurons for the upper face project to the facial nuclei bilaterally. Therefore, upper motor neuron lesions, such as a stroke, cause contralateral face weakness sparing the forehead, while lower motor neuron lesions, such as a facial nerve injury, typically cause weakness involving the whole ipsilateral face.

35. Cranial Nerve 8 Hearing and Balance
Test to see can the patient hear fingers rubbed together or words whispered just outside of the auditory canal and identify which ear hears the sound? A tuning fork can be used to perform the Weber and Rinne test to evaluate sensorineural and conductive hearing loss respectively
Hearing loss can be caused by lesions in the acoustic and mechanical elements of the ear, the neural elements of the cochlea, or the acoustic nerve (CN VIII). After the hearing pathways enter the brainstem, they cross over at multiple levels and ascend bilaterally to the thalamus and auditory cortex. Therefore, clinically significant unilateral hearing loss is invariably caused by peripheral neural or mechanical lesions.
Vestibular testing is not done routinely.

36. CRANIAL NERVES IX/X - GLOSSOPHARYNGEAL, VAGUS XI - SPINAL ACCESSORY
GAG
XI - SPINAL ACCESSORY
STERNOCLEIDOMASTOID M.
TRAPEZIUS MUSCLE
XII - HYPOGLOSSAL
TONGUE STRENGTH
RIGHT XII THRUSTS TONGUE TO LEFT

37. Cranial Nerve 9 and 10 Palatal Elevation and Gag Reflex
Does the palate elevate symmetrically when the patient says, "Aah"? Does the patient gag when the posterior pharynx is brushed? The gag reflex needs to be tested only in patients with suspected brainstem pathology, impaired consciousness, or impaired swallowing.
Palate elevation and the gag reflex are impaired in lesions involving CN 9, CN 10, the neuromuscular junction, or the pharyngeal muscles.

38. Cranial Nerve11 Sternocleidomastoid and Trapezius Muscles
Ask the patient to shrug their shoulders, turn their head in both directions, and raise their head from the bed, flexing forward against the force of your hands.
Weakness in the sternocleidomastoid or trapezius muscles can be caused by lesions in the muscles, neuromuscular junction, or lower motor neurons of the accessory spinal nerve (CN XI). Unilateral upper motor neuron lesions in the cortex or descending pathways cause contralateral weakness of the trapezius, with relative sparing of sternocleidomastoid strength

39. Cranial Nerve12
Note any atrophy or fasciculations (spontaneous quivering movements caused by firing of muscle motor units) of the tongue while it is resting on the floor of the mouth. Ask the patient to stick their tongue straight out and note whether it curves to one side or the other. Ask the patient to move their tongue from side to side and push it forcefully against the inside of each cheek
Fasciculations and atrophy are signs of lower motor neuron lesions. Unilateral tongue weakness causes the tongue to deviate toward the weak side. Tongue weakness can result from lesions of the tongue muscles, the neuromuscular junction, the lower motor neurons of the hypoglossal nerve (CN XII), or the upper motor neurons originating in the motor cortex. Lesions of the motor cortex cause contralateral tongue weakness.

40. Hypoglossal Nerve Injury

41. MOTOR EXAMINATION

42. Motor Examination

43. Motor Examination
Observe: Look for any twitches, tremors, abnormal movements or postures. Look carefully for hypokinesia,decreased eye blinking or staring which could be indicative or an extrapyramidal disorder such as Parkinson’s disease
In suspected lower motor neuron disorders,look for muscle wasting or fasiculations
Palpate muscles in cases of suspected myopathy to check for muscle tenderness
Passively move each limb to check muscle tone. Ask the patient to relax before beginning

44. MUSCLE OBSERVATION
ATROPHY
FASCIULATIONS

45. ABNORMAL MOVEMENTS TREMOR CHOREA ATHETOSIS ABNORMAL POSTURES REST
WITH ARMS OUTSTRETCHED
INTENTION
CHOREA
ATHETOSIS
ABNORMAL POSTURES

46. TONE
INCREASED, DECREASED, NORMAL
COGWHEELING
CLASP KNIFE

47. Motor Examination
Test for subtle weakness first by checking pronator drift, finger tapping, pronation/supination movements and toe tapping.
Then check individual muscles for strength using the MRC scale to rate strength

48. STRENGTH STRENGTH GRADED 0 - 5 0 - NO MOVEMENT 1 - FLICKER
2 - MOVEMENT WITH GRAVITY REMOVED
3 - MOVEMENT AGAINST GRAVITY
4 - MOVEMENT AGAINST RESISTANCE
5 - NORMAL STRENGTH

49. STRENGTH EXAM UPPER AND LOWER EXTREMITIES DISTAL AND PROXIMAL MUSCLES
GRIP STRENGTH IS A POOR SCREENING TOOL FOR STRENGTH
SUBTLE WEAKNESS
TOE WALK, HEEL WALK
OUT OF CHAIR
DEEP KNEE BEND

50. REFLEXES

51. MUSCLE STRETCH REFLEXES (DEEP TENDON REFLEXES)
GRADED 0 - 5
0 - ABSENT
1 - PRESENT WITH REINFORCEMENT
2 - NORMAL
3 - ENHANCED
4 - UNSUSTAINED CLONUS
5 - SUSTAINED CLONUS

52. MSR / DTR
BICEPS
BRACHIORADIALIS
TRICEPS
KNEE
ANKLE

53. OTHER REFLEXES Upper motor neuron dysfunction Frontal release signs
BABINSKI
present or absent
toes downgoing/ flexor plantar response
HOFMAN’S
JAW JERK
Frontal release signs
GRASP
SNOUT
SUCK
PALMOMENTAL

54. Plantar Response
Test the plantar response by scraping an object across the sole of the foot beginning from the heel, moving forward toward the small toe, and then arcing medially toward the big toe. The normal response is downward contraction of the toes. The abnormal response, called Babinski's sign, is characterized by an upgoing big toe and fanning outward of the other toes.The presence of Babinski's sign is always abnormal in adults, but it is often present in infants, up to the age of about 1 year.

56. CEREBELLAR FUNCTION RAPID ALTERNATING MOVEMENTS
FINGER TO FINGER TO NOSE TESTING
HEEL TO SHIN
GAIT
TANDEM

57. Coordination
Normal performance of these motor tasks depends on the integrated functioning of multiple sensory and motor subsystems. These include position sense pathways, lower motor neurons, upper motor neurons, the basal ganglia, and the cerebellum. Thus, in order to convincingly demonstrate that abnormalities are due to a cerebellar lesion, one must first test for normal joint position sense, strength, and reflexes and confirm the absence of involuntary movements caused by basal ganglia lesions. As already mentioned, limb ataxia is usually caused by lesions of the cerebellar hemispheres and associated pathways, while truncal ataxia is often caused by damage to the midline cerebellar vermis and associated pathway
Tests for Limb Ataxia include: Rapid alternating movements, Finger Nose Finger test, and Heel Knee Shin test

58. Gait evaluation Include walking and turning Examples of abnormal gait
High steppage
Waddling
Hemiparetic
Shuffling
Turns en bloc

59. Gait
Gait involves multiple sensory and motor systems. These include vision, proprioception, lower motor neurons, upper motor neurons, basal ganglia, the cerebellum, and higher-order motor planning systems in the association cortex
Observe:
Stance, how far apart are the feet, posture, stability, how high the feet are raised off the floor, trajectory of leg swing and whether there is circumduction (an arced trajectory in the medial to lateral direction), leg stiffness and degree of knee bending, arm swing, tendency to fall or swerve in any particular direction, rate and speed, difficulty initiating or stopping gait, and any involuntary movements that are brought out by walking. Turns should also be observed closely. The patient's ability to rise from a chair with or without assistance should also be recorded.
To bring out abnormalities in gait and balance, ask the patient to do more difficult maneuvers : ie Tandem Gait

60. Romberg Sign
Stand with feet together - assure patient stable - have them close eyes
Romberg is positive if they do worse with eyes closed
Measures
Cerebellar function
Frequently poor balance with eyes open and closed
Proprioception
Frequently do worse with eyes closed
Vestibular system

61. SENSORY EXAM

62. Sensory Exam
The sensory exam relies to a large extent on the ability or willingness of the patient to report what he is feeling. It can therefore often be the most difficult and unreliable part of the neurologic exam

63. Primary Sensation Light Touch Pinprick Vibration Joint Position
Temperature
Two point discrimination
The pattern of sensory loss can provide important information that helps localize lesions to particular nerves, nerve roots, and regions of the spinal cord, brainstem, thalamus, or cortex

64. SENSORY EXAM VIBRATION JOINT POSITION SENSE PIN PRICK TEMPERATURE
128 hz tuning fork
JOINT POSITION SENSE
PIN PRICK
TEMPERATURE
Start distally and move proximally

65. HIGHER CORTICAL SENSATIONS
GRAPHESTHESIA
STEREOGNOSIS
DOUBLE SIMULTANEOUS STIMULATION
BAROSTHESIA
TEXTURES

66. Cortical sensation Graphesthesia Sterognosis
Double Simultaneous Stimulation
Intact primary sensation with deficits in cortical sensation such as agraphesthesia or astereognosis suggests a lesion in the contralateral sensory cortex. Note, however, that severe cortical lesions can cause deficits in primary sensation as well. Extinction with intact primary sensation is a form of hemineglect that is most commonly associated with lesions of the right parietal lobe. Extinction can also be seen in right frontal or subcortical lesions, or sometimes in left hemisphere lesions causing mild right hemineglect