Variant ABeta2M amyloidosis

MONDO:0017810

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

27 clinical trials for this condition and its sub-types.

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