Achievable logoAchievable logo
NPTE-PT
Sign in
Sign up
Purchase
Textbook
Practice exams
Support
How it works
Exam catalog
Mountain with a flag at the peak
Textbook
Introduction
1. Cardiopulmonary system
2. Pulmonary system
3. Neuromuscular system
3.1 Central nervous system
3.2 Anatomy and function of spinal cord
3.3 Peripheral nervous system
3.4 Differential diagnosis of central nervous system pathologies
3.5 Differential diagnosis of peripheral nervous system
3.6 Other neurological conditions
3.7 Interventions for neurological conditions
3.8 Vestibular system
4. Pediatrics
5. Musculoskeletal system
6. Other system
7. Non-systems
Wrapping up
Achievable logoAchievable logo
3.5 Differential diagnosis of peripheral nervous system
Achievable NPTE-PT
3. Neuromuscular system
Our NPTE-PT course is currently in development and is a work-in-progress.

Differential diagnosis of peripheral nervous system

3 min read
Font
Discuss
Share
Feedback

Peripheral nerve injuries

Injuries to the peripheral nerves due to trauma, chronic traction, compression, or shear

Definitions
Wallerian degeneration
Degeneration of the axon and myelin sheath distal to the site of an axonal interruption
Neuropathy
Degenerative changes in peripheral nerves that produce loss of motor and sensory function; caused by diabetes, nutritional deficits, or alcohol use
Mononeuropathy
Degeneration of a single nerve
Polyneuropathy
Bilateral, symmetrical involvement of peripheral nerves typically in stoking/glove distribution
Neuropraxia
Injury to nerve causing sudden loss of function (compression injury); dysfunction can be rapidly reversed or persist for weeks
Axontomesis
Injury to nerve interrupting the axon and causing loss of function and degeneration distal to the lesion (crush injury); regeneration is possible with or without surgical intervention
Neurotomesis
Cutting the nerve from all structure and complete loss of function; reinnervation fails without surgical intervention
Entrapment syndrome
Pressure on nerve where it passes through an opening or over a bony prominence

Myasthenia gravis

An autoimmune disorder leading to decreased acetylcholine receptors at the neuromuscular junction and thus a decrease in muscular contraction with repetition.

Symptoms:

  • Muscle weakness, especially in the eyes, face, throat, and limbs
  • Double vision
  • Drooping eyelids
  • Difficulty swallowing or speaking
  • Weakness that worsens with activity and improves with rest

Myasthenia crisis occurs when exacerbation of symptoms progresses to the respiratory system leading to life-threatening weakness.

Interventions for myasthenia gravis

  • Energy conservation techniques are goal of sessions
    • No strength training as patient becomes more fatigued with increased repetition of activity
  • Attempt to conduct therapy sessions in morning to decrease fatigue
  • Avoid thermal modalities such as heat packs, whirlpool, etc.

Bell’s palsy

A lower motor neuron lesion involving cranial nerve VII (facial nerve) causing unilateral facial paralysis due to acute inflammation of unknown etiology resulting in compression of nerve in temporal bone. Symptoms are worst within the first few hours or days leading to symptoms lasting for several weeks or months.

Symptoms

  • Facial droop on one side of face
  • Drooling from one side
  • Loss of taste to anterior 2/3 of tongue
  • Changes in saliva and tear production
  • Headache
  • Loss of sensation to anterior two-thirds of tongue
  • Sensory to face remains intact

Interventions for Bell’s palsy

  • Spontaneous recovery can occur
  • Corticosteroid use for inflammation
  • Electrical-stimulation for nerve stimulation
  • Exercises for facial muscles
  • Taping of eyelid to prevent dry eye due to inability to close eyelid

Guillain-Barré syndrome (GBS)

An acute autoimmune disorder in which peripheral nerves are damaged. Typically, occurs after recovery from viral illness causing demyelination to both cranial and peripheral nerves.

Symptoms

  • Causes motor and sensory loss distal to proximal in symmetrical pattern
  • Usually begins in the legs and will extend towards trunk/UE
  • Worse prognosis if reaching lungs and need for mechanical ventilation
  • Motor/sensory loss progressively worsens over 4 week period and then stabilizes

Interventions for Guillain-Barré syndrome

  • Sessions focus on compensatory strategies to assist with gait and mobility
  • Avoidance of overstretching and overuse during acute phases of diagnosis
  • Strength training performed once stabilization of disease process occurs with progression from isometric to concentric to eccentric activities

Peripheral nerve injuries

  • Caused by trauma, traction, compression, or shear
  • Key terms:
    • Wallerian degeneration: distal axon/myelin breakdown after injury
    • Neuropathy: loss of motor/sensory function from nerve degeneration
    • Mononeuropathy: single nerve involvement
    • Polyneuropathy: bilateral, symmetrical nerve involvement (stocking/glove)
    • Neuropraxia: reversible nerve function loss (compression)
    • Axontomesis: axon interrupted, distal degeneration, possible regeneration
    • Neurotomesis: complete nerve cut, no reinnervation without surgery
    • Entrapment syndrome: nerve pressure at anatomical passage

Myasthenia gravis

  • Autoimmune loss of acetylcholine receptors at neuromuscular junction
  • Symptoms: muscle weakness (eyes, face, throat, limbs), worsens with activity, improves with rest
  • Myasthenic crisis: respiratory muscle weakness, life-threatening
  • Interventions:
    • Energy conservation, avoid strength training
    • Morning therapy sessions preferred
    • Avoid heat modalities

Bell’s palsy

  • Lower motor neuron lesion of cranial nerve VII (facial nerve)
  • Unilateral facial paralysis, acute onset, often recovers spontaneously
  • Symptoms: facial droop, drooling, loss of anterior tongue taste, altered saliva/tear production, intact facial sensation
  • Interventions:
    • Corticosteroids for inflammation
    • Electrical stimulation and facial muscle exercises
    • Eyelid taping to prevent dry eye

Guillain-Barré syndrome (GBS)

  • Acute autoimmune demyelination of cranial and peripheral nerves, often post-viral
  • Symptoms: symmetrical distal-to-proximal motor/sensory loss, may require ventilation if respiratory muscles involved, progression over 4 weeks then stabilization
  • Interventions:
    • Compensatory strategies for mobility/gait
    • Avoid overstretching/overuse during acute phase
    • Gradual strength training after stabilization (isometric → concentric → eccentric)
Previous
Next  | 3.6 Other neurological conditions
All rights reserved ©2016 - 2026 Achievable, Inc.

Differential diagnosis of peripheral nervous system

Peripheral nerve injuries

Injuries to the peripheral nerves due to trauma, chronic traction, compression, or shear

Definitions
Wallerian degeneration
Degeneration of the axon and myelin sheath distal to the site of an axonal interruption
Neuropathy
Degenerative changes in peripheral nerves that produce loss of motor and sensory function; caused by diabetes, nutritional deficits, or alcohol use
Mononeuropathy
Degeneration of a single nerve
Polyneuropathy
Bilateral, symmetrical involvement of peripheral nerves typically in stoking/glove distribution
Neuropraxia
Injury to nerve causing sudden loss of function (compression injury); dysfunction can be rapidly reversed or persist for weeks
Axontomesis
Injury to nerve interrupting the axon and causing loss of function and degeneration distal to the lesion (crush injury); regeneration is possible with or without surgical intervention
Neurotomesis
Cutting the nerve from all structure and complete loss of function; reinnervation fails without surgical intervention
Entrapment syndrome
Pressure on nerve where it passes through an opening or over a bony prominence

Myasthenia gravis

An autoimmune disorder leading to decreased acetylcholine receptors at the neuromuscular junction and thus a decrease in muscular contraction with repetition.

Symptoms:

  • Muscle weakness, especially in the eyes, face, throat, and limbs
  • Double vision
  • Drooping eyelids
  • Difficulty swallowing or speaking
  • Weakness that worsens with activity and improves with rest

Myasthenia crisis occurs when exacerbation of symptoms progresses to the respiratory system leading to life-threatening weakness.

Interventions for myasthenia gravis

  • Energy conservation techniques are goal of sessions
    • No strength training as patient becomes more fatigued with increased repetition of activity
  • Attempt to conduct therapy sessions in morning to decrease fatigue
  • Avoid thermal modalities such as heat packs, whirlpool, etc.

Bell’s palsy

A lower motor neuron lesion involving cranial nerve VII (facial nerve) causing unilateral facial paralysis due to acute inflammation of unknown etiology resulting in compression of nerve in temporal bone. Symptoms are worst within the first few hours or days leading to symptoms lasting for several weeks or months.

Symptoms

  • Facial droop on one side of face
  • Drooling from one side
  • Loss of taste to anterior 2/3 of tongue
  • Changes in saliva and tear production
  • Headache
  • Loss of sensation to anterior two-thirds of tongue
  • Sensory to face remains intact

Interventions for Bell’s palsy

  • Spontaneous recovery can occur
  • Corticosteroid use for inflammation
  • Electrical-stimulation for nerve stimulation
  • Exercises for facial muscles
  • Taping of eyelid to prevent dry eye due to inability to close eyelid

Guillain-Barré syndrome (GBS)

An acute autoimmune disorder in which peripheral nerves are damaged. Typically, occurs after recovery from viral illness causing demyelination to both cranial and peripheral nerves.

Symptoms

  • Causes motor and sensory loss distal to proximal in symmetrical pattern
  • Usually begins in the legs and will extend towards trunk/UE
  • Worse prognosis if reaching lungs and need for mechanical ventilation
  • Motor/sensory loss progressively worsens over 4 week period and then stabilizes

Interventions for Guillain-Barré syndrome

  • Sessions focus on compensatory strategies to assist with gait and mobility
  • Avoidance of overstretching and overuse during acute phases of diagnosis
  • Strength training performed once stabilization of disease process occurs with progression from isometric to concentric to eccentric activities
Key points

Peripheral nerve injuries

  • Caused by trauma, traction, compression, or shear
  • Key terms:
    • Wallerian degeneration: distal axon/myelin breakdown after injury
    • Neuropathy: loss of motor/sensory function from nerve degeneration
    • Mononeuropathy: single nerve involvement
    • Polyneuropathy: bilateral, symmetrical nerve involvement (stocking/glove)
    • Neuropraxia: reversible nerve function loss (compression)
    • Axontomesis: axon interrupted, distal degeneration, possible regeneration
    • Neurotomesis: complete nerve cut, no reinnervation without surgery
    • Entrapment syndrome: nerve pressure at anatomical passage

Myasthenia gravis

  • Autoimmune loss of acetylcholine receptors at neuromuscular junction
  • Symptoms: muscle weakness (eyes, face, throat, limbs), worsens with activity, improves with rest
  • Myasthenic crisis: respiratory muscle weakness, life-threatening
  • Interventions:
    • Energy conservation, avoid strength training
    • Morning therapy sessions preferred
    • Avoid heat modalities

Bell’s palsy

  • Lower motor neuron lesion of cranial nerve VII (facial nerve)
  • Unilateral facial paralysis, acute onset, often recovers spontaneously
  • Symptoms: facial droop, drooling, loss of anterior tongue taste, altered saliva/tear production, intact facial sensation
  • Interventions:
    • Corticosteroids for inflammation
    • Electrical stimulation and facial muscle exercises
    • Eyelid taping to prevent dry eye

Guillain-Barré syndrome (GBS)

  • Acute autoimmune demyelination of cranial and peripheral nerves, often post-viral
  • Symptoms: symmetrical distal-to-proximal motor/sensory loss, may require ventilation if respiratory muscles involved, progression over 4 weeks then stabilization
  • Interventions:
    • Compensatory strategies for mobility/gait
    • Avoid overstretching/overuse during acute phase
    • Gradual strength training after stabilization (isometric → concentric → eccentric)

More from Neuromuscular system

  • Central nervous system
  • Anatomy and function of spinal cord
  • Peripheral nervous system
  • Differential diagnosis of central nervous system pathologies
  • Other neurological conditions