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  2. Alcoholic polyneuropathy - Wikipedia

    en.wikipedia.org/wiki/Alcoholic_polyneuropathy

    Alcoholic polyneuropathy usually has a gradual onset over months or even years, although axonal degeneration often begins before an individual experiences any symptoms. [ 2 ] The disease typically involves sensory issues and motor loss, as well as painful physical perceptions, though all sensory modalities may be involved. [ 3 ]

  3. Acute motor axonal neuropathy - Wikipedia

    en.wikipedia.org/wiki/Acute_motor_axonal_neuropathy

    Acute motor axonal neuropathy (AMAN) is a variant of Guillain–Barré syndrome. It is characterized by acute paralysis and loss of reflexes without sensory loss. Pathologically , there is motor axonal degeneration with antibody-mediated attacks of motor nerves and nodes of Ranvier .

  4. Polyneuropathy - Wikipedia

    en.wikipedia.org/wiki/Polyneuropathy

    This demyelination slows down or completely blocks the conduction of action potentials through the axon of the nerve cell (neurapraxia). [12] The most common cause is acute inflammatory demyelinating polyneuropathy AIDP, the most common form of Guillain–Barré syndrome [ 13 ] (although other causes include chronic inflammatory demyelinating ...

  5. Sensory neuronopathy - Wikipedia

    en.wikipedia.org/wiki/Sensory_neuronopathy

    Sensory neuronopathy differs from the more common length dependent axonal polyneuropathies (such as diabetic sensorimotor polyneuropathy) in that the symptoms do not progress in a distal to proximal pattern (starting in the feet and progressing to the legs and hands), rather symptoms develop in a multifocal, asymmetric, and non-length dependent ...

  6. Hereditary motor and sensory neuropathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_motor_and...

    Symptoms of these disorders include: fatigue, pain, lack of balance, lack of feeling, lack of reflexes, and lack of sight and hearing, which result from muscle atrophy. Patients can also have high arched feet, hammer toes, foot drop, foot deformities, and scoliosis. These symptoms are a result of severe muscular weakness and atrophy.

  7. Demyelinating disease - Wikipedia

    en.wikipedia.org/wiki/Demyelinating_disease

    N-cadherin agonists have been identified and observed to stimulate neurite growth and cell migration, key aspects of promoting axon growth and remyelination after injury or disease. [ 25 ] Immunomodulatory drugs such as fingolimod have been shown to reduce immune-mediated damage to the CNS, preventing further damage in patients with MS.

  8. Ulnar neuropathy - Wikipedia

    en.wikipedia.org/wiki/Ulnar_neuropathy

    In regards to the pathophysiology of ulnar neuropathy:the axon, and myelin can be affected. Within the axon, fascicles to individual muscles could be involved, with subsequent motor unit loss and amplitude decrease. Conduction block means impaired transmission via a part of the nerve.

  9. Pathophysiology of nerve entrapment - Wikipedia

    en.wikipedia.org/wiki/Pathophysiology_of_nerve...

    The axon's survival depends on its connection with the cell body, supported by the axonal transport mechanisms to carry cellular material. [4] The axonal transport system carries material along the axon in both directions (anterograde and retrograde) at different speeds (fast and slow). [4] [5] The fast transport travels at up to 400 mm/day.