Conditions / Genetic

variant ABeta2M amyloidosis

info · Genetic

An amyloidosis that is 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