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Amyloid Neuropathies

More information in Books or onNLM PubMed
Definition: Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)  coord IM with specific neurol dis (IM) or specific nerve (IM); /genet: consider also AMYLOID NEUROPATHIES, FAMILIAL   
Examples Amyloid Neuropathies, Familial
Other names Neuropathies, Amyloid; Secondary Amyloid Neuropathy; Secondary Amyloid Neuropathies; Polyneuropathy, Amyloid; Polyneuropathies, Amyloid; Neuropathy, Secondary Amyloid; Neuropathy, Amyloid; Neuropathies, Secondary Amyloid; Amyloid Polyneuropathy; Amyloid Neuropathy; Amyloid Neuropathies, Secondary; Amyloid Polyneuropathies; Amyloid Neuropathy, Secondary
 
SubstanceCAS Registry & nameCategoriesSource
Amyloid Neuropathies, Primary (nonfamilial)  0   *Amyloid Neuropathies.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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