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