Structured Summary
Abstract
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)
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Synonyms
13 entry terms
- Amyloid Polyneuropathies
- Neuropathies, Amyloid
- Amyloid Neuropathy
- Amyloid Polyneuropathy
- Neuropathy, Amyloid
- Polyneuropathies, Amyloid
- Polyneuropathy, Amyloid
- Amyloid Neuropathy, Secondary
- Amyloid Neuropathies, Secondary
- Neuropathies, Secondary Amyloid
- Neuropathy, Secondary Amyloid
- Secondary Amyloid Neuropathies
- Secondary Amyloid Neuropathy
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Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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Indexing Annotation
coord IM with specific neurol dis (IM) or specific nerve (IM); /genet: consider also AMYLOID NEUROPATHIES, FAMILIAL
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History Note
1994
MeSH Record
Previous Indexing
- Amyloidosis (1967-1993)
- Peripheral Nervous System Diseases (1967-1993)
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References
- National Library of Medicine. Amyloid Neuropathies. Medical Subject Headings (MeSH). 2026. Unique ID D017772. http://id.nlm.nih.gov/mesh/2026/D017772
- Amyloid Neuropathies. In: Wikidata. https://www.wikidata.org/wiki/Q54911710