2.3 Neurological Conditions
Key Takeaways
MCA stroke causes contralateral hemiplegia (arm/face > leg), aphasia (dominant hemisphere), and neglect (non-dominant); ACA stroke spares the face and affects the leg more
SCI functional levels: C4 ventilator-dependent, C5 deltoid/biceps, C6 tenodesis grasp, C7 independent transfers, C8-T1 full hand, lower levels add ambulation
Parkinson disease shows the TRAP signs: resting tremor, rigidity, akinesia/bradykinesia, and postural instability
Multiple sclerosis is CNS demyelination; relapsing-remitting is most common and symptoms worsen with heat (Uhthoff phenomenon)
TBI recovery is tracked with the Rancho Los Amigos Levels (I-VIII), from no response to purposeful-appropriate behavior
Guillain-Barre is an ascending demyelinating LMN polyneuropathy; respiratory and autonomic failure are the dangerous complications
BPPV is the most common vestibular disorder and is treated with canalith repositioning (Epley maneuver)
ALS degenerates both UMN and LMN, is progressive and fatal, and PT focuses on preserving function and safety
The NPTE tests recognition, expected function, and PT management of major neurological conditions. This section covers the highest-yield ones.
Stroke (Cerebrovascular Accident)
By artery
| Artery | Region | Presentation |
|---|---|---|
| MCA | Lateral hemisphere | Contralateral hemiplegia (arm/face > leg), sensory loss, aphasia (dominant), neglect (non-dominant), homonymous hemianopsia |
| ACA | Medial hemisphere | Contralateral hemiplegia (leg > arm), personality change, incontinence |
| PCA | Occipital, medial temporal | Homonymous hemianopsia, memory and visual deficits |
| Vertebrobasilar | Brainstem, cerebellum | Ataxia, vertigo, cranial-nerve signs, dysphagia, locked-in syndrome |
Aphasia (dominant/left hemisphere)
| Type | Fluency | Comprehension | Lesion |
|---|---|---|---|
| Broca (expressive) | Non-fluent | Intact | Frontal (Broca area) |
| Wernicke (receptive) | Fluent but nonsensical | Impaired | Temporal (Wernicke area) |
| Global | Non-fluent | Impaired | Large MCA territory |
Brunnstrom recovery progresses through 7 stages: flaccidity (1), emerging spasticity/synergies (2), peak spasticity (3), spasticity declining with movement out of synergy (4), more isolated movement (5), near-normal coordination (6), and normal (7).
Spinal Cord Injury (SCI)
Functional levels (complete injury)
| Level | Key muscle | Functional expectation |
|---|---|---|
| C1-C3 | None (diaphragm out) | Ventilator-dependent, power w/c with head control |
| C4 | Diaphragm | May wean from vent; power w/c (chin/sip-and-puff) |
| C5 | Deltoid, biceps | Feeding with setup; power or adapted manual w/c |
| C6 | Wrist extensors | Tenodesis grasp; modified-independent ADLs; manual w/c on level |
| C7 | Triceps | Independent transfers and manual w/c; most ADLs |
| C8-T1 | Hand intrinsics | Independent ADLs and fine motor |
| T6-T12 | Trunk (progressive) | Improving trunk control; standing frame |
| L2-L4 | Hip flexors, quads | Household ambulation with orthoses |
| L5-S1 | Ankle muscles | Community ambulation, often with an AFO |
Incomplete syndromes
| Syndrome | Lesion | Presentation |
|---|---|---|
| Central cord | Central gray | UE weakness > LE, cape-like sensory loss |
| Anterior cord | Anterior 2/3 | Motor + pain/temp loss; proprioception spared |
| Brown-Sequard | Cord hemisection | Ipsilateral motor + proprioception loss; contralateral pain/temp loss |
| Posterior cord | Dorsal columns | Proprioception/vibration loss; motor and pain/temp spared |
| Cauda equina | Roots below conus | LMN signs, saddle anesthesia, bowel/bladder dysfunction |
Watch for autonomic dysreflexia in injuries at or above T6: a noxious stimulus below the lesion (often a blocked catheter) triggers a hypertensive emergency. The PT immediately sits the patient upright and removes the trigger.
Parkinson Disease, MS, and TBI
Parkinson disease results from loss of dopaminergic neurons in the substantia nigra. The cardinal TRAP signs are resting (pill-rolling) Tremor, cogwheel/lead-pipe Rigidity, Akinesia/bradykinesia, and Postural instability. The gait is shuffling and festinating (short, accelerating steps) with reduced arm swing, forward lean, and freezing, especially at doorways and turns.
Multiple sclerosis is autoimmune demyelination of CNS white matter. Relapsing-remitting MS (~85% at onset) is most common; many later convert to secondary-progressive. Key NPTE pearls: Uhthoff phenomenon (symptoms worsen with heat), Lhermitte sign (electric shock down the spine with neck flexion), and the avoid-overheating precaution—keep aquatic-therapy water cool (around or below ~29 C / 85 F) and use energy conservation for fatigue.
Traumatic brain injury recovery is staged with the Rancho Los Amigos Levels of Cognitive Functioning (I-VIII), from Level I (no response) through Level IV (confused-agitated) to Level VIII (purposeful-appropriate). PT structures the environment for low-level/agitated patients and progressively challenges cognition and mobility as the patient advances.
Guillain-Barre, Vestibular Disorders, and ALS
Guillain-Barre syndrome (GBS) is an acute inflammatory demyelinating polyneuropathy producing ascending, symmetric LMN weakness (flaccidity, areflexia), often after an infection. The danger is respiratory failure (monitor vital capacity) and autonomic instability. PT emphasizes positioning, gentle non-fatiguing exercise during recovery, and respiratory care; overexertion early can worsen outcomes.
Vestibular disorders cause vertigo, nystagmus, and imbalance. Benign paroxysmal positional vertigo (BPPV)—otoconia displaced into a semicircular canal—is the most common and is treated with canalith repositioning (the Epley maneuver), not with prolonged rest. Unilateral vestibular hypofunction is treated with vestibular rehabilitation (gaze-stabilization and habituation exercises).
Amyotrophic lateral sclerosis (ALS) degenerates both UMN and LMN, producing a mixed picture (spasticity plus atrophy/fasciculations) that progresses to respiratory failure and is ultimately fatal. PT is not curative: it focuses on preserving function and safety, energy conservation, equipment and assistive devices, and avoiding overwork weakness while supporting quality of life.
Tying Presentation to PT Priorities
For each condition, the exam wants the priority that flows from the pathology. After stroke, prevent learned non-use and train tasks. In SCI, predict function by level and guard against complications such as autonomic dysreflexia (T6 and above), pressure injuries, and orthostatic hypotension. In Parkinson disease, use external cueing and large-amplitude movement to counter bradykinesia and freezing. In MS, conserve energy and avoid overheating. In GBS, monitor respiration and avoid overexertion during recovery. In ALS, preserve function and prevent overwork fatigue rather than chase strength gains.
Pairing each diagnosis with its single highest PT priority converts a long list of diseases into a small set of decision rules the exam rewards.
Recovery Expectations and Prognosis
The exam also probes realistic prognosis. After stroke, the fastest motor recovery occurs in the first weeks to months, though gains continue longer with training. Complete (ASIA A) SCI carries a guarded prognosis for motor return below the level, whereas incomplete injuries have more potential. Progressive diseases (MS, Parkinson, ALS) require goals framed around maintaining function and safety and adapting as the disease evolves, not curing.
Matching your goal-setting and family education to each condition's expected trajectory is itself a tested competency, and it guides whether the plan emphasizes restoration, compensation, or maintenance.
A patient has contralateral hemiplegia (arm > leg), Broca aphasia, and homonymous hemianopsia. The stroke is MOST likely in the:
Middle cerebral artery
Anterior cerebral artery
Posterior cerebral artery
Cerebellum
A patient with a complete C6 spinal cord injury would be expected to:
Be ventilator-dependent
Have full hand intrinsic function
Walk with bilateral AFOs
Have a functional tenodesis grasp and be modified-independent in many ADLs
Which is characteristic of Parkinson disease gait?
Shuffling, festinating gait with reduced arm swing
Wide-based ataxic gait
High-steppage gait
Antalgic gait with shortened stance
An MS patient reports symptoms worsen during a hot bath. This is:
Lhermitte sign
A pseudo-relapse from infection only
Autonomic dysreflexia
Uhthoff phenomenon
Brown-Sequard syndrome (cord hemisection) produces:
Ipsilateral motor and proprioception loss with contralateral pain/temperature loss
Bilateral motor and sensory loss below the lesion
Loss of pain and temperature only
UE weakness greater than LE weakness
The Parkinson cardinal signs are remembered by TRAP: Tremor, Rigidity, Akinesia/Bradykinesia, and Postural _____.
Type your answer below
Central cord syndrome typically presents with:
Arm weakness greater than leg weakness, with a cape-like sensory loss
Leg weakness greater than arm weakness
Pure proprioceptive loss
Saddle anesthesia and bowel/bladder loss
BPPV (benign paroxysmal positional vertigo) is MOST effectively treated with:
The Epley canalith-repositioning maneuver
Strict bed rest
Vestibular suppressant medication indefinitely
Cervical traction
In an SCI at or above T6, a sudden pounding headache and severe hypertension from a blocked catheter indicates autonomic dysreflexia. The PT should FIRST:
Sit the patient upright and remove the noxious stimulus
Lay the patient flat and elevate the legs
Begin aggressive aerobic exercise
Apply ice to the lower extremities
Sections you finish are checked off in the contents.