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Variant ABeta2M amyloidosis

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Name:
Variant ABeta2M amyloidosis
Description:
A rare form of amyloidosis characterized by accumulation and extensive visceral deposition of anamyloidogenic variant of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy.
ORPHAcode:
314652
Synonyms:
Autosomal dominant beta2-microglobulinic amyloidosis
XREF(s):
Orphanet
ICD-10
Analyte(s):
B2M
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14