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Classifications:
Neuropraxia (Sunderland 1°)
Axonotmesis (Sunderland 2° and 3°)
Neurotmesis (Sunderland 3°, 4°, and 5°)
Segmental demyelination
Action potential slowed or blocked at point of demyelination; normal above and below point of compression
The result of mild ischemia from nerve compression or traction
Neuropraxia (Sunderland 1°)
Signs and symptoms of Neuropraxia (Sunderland 1°):
Pain
No or minimal muscle wasting
Muscle weakness
Numbness
Proprioception affected
Recovery time for Neuropraxia (Sunderland 1°):
Minutes to days
Loss of axonal continuity but connective tissue coverings remain intact
Wallerian degeneration distal to lesion
The result of prolonged compression or stretch causing infarction and necrosis
Axonotmesis (Sunderland 2° and 3°)
Signs and symptoms of Axonotmesis (Sunderland 2° and 3°):
Pain
Muscle wasting evident
Complete motor, sensory and sympathetic functions lost
Sensation is restored before motor function
Recovery time for Axonotmesis (Sunderland 2° and 3°):
Months (axon regenerates at rate of 1 inch/month, or 1 mm/day)
Complete severance of nerve fiber with disruption of connective tissue coverings
Wallerian degeneration distal to lesion
The result of gunshot or stab wounds, avulsion, rupture
Neurotmesis (Sunderland 3°, 4°, and 5°)
Signs and symptoms of Neurotmesis (Sunderland 3°, 4°, and 5°):
No pain (anesthesia)
Muscle wasting
Complete motor, sensory and sympathetic functions lost
Recovery time for Neurotmesis (Sunderland 3°, 4°, and 5°):
Months and only with surgery