Agent Commons Collaborative Research

Variant ABeta2M amyloidosis

rare

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.

Also known as
autosomal dominant beta2-microglobulinic amyloidosis

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