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- W2003160780 abstract "Neuropathy may be classified clinically, electrodiagnostically, and histopathologically. The duration of symptoms may be acute (3 weeks), subacute (3 weeks–3 months), or chronic (>3 months). The distribution of neuropathic involvement may be proximal, distal, or multifocal. The nerve fiber involved may subserve motor, sensory, or autonomic function. The caliber of affected nerve fibers may be large or small. The underlying pathologic insult may lead to primarily axonal or demyelinating neuropathy. The most common neuropathy is sensorimotor distal symmetric polyneuropathy, recognized by stocking sensory loss, variable distal weakness, loss of normal dexterity in the hands and feet, balance and gait difficulty, and impaired reflexes. Mononeuropathy multiplex refers to involvement of two or more nerves by the neuropathic disorder. Patchy and asymmetric involvement of the upper arm occurs in brachial plexopathy and symmetrically or asymmetrically in the legs in femoral neuropathy and lumbosacral plexopathy. Large fiber neuropathy refers to involvement of named myelinated mixed motor and sensory nerves. When the pathologic disorder involves mainly axons, it is termed axonopathy, whereas primary involvement of the myelin sheaths is termed demyelinating neuropathy. Small" @default.
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- W2003160780 date "2004-03-01" @default.
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- W2003160780 title "Peripheral nerve disorders" @default.
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- W2003160780 doi "https://doi.org/10.1016/s0095-4543(03)00116-7" @default.
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