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The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 85450
A group of rare renal diseases, characterized by amyloid fibril deposition of apolipoprotein A-I or A-II (AApoAI or AApoAII amyloidosis), lysozyme (ALys amyloidosis) or fibrinogen A-alpha chain (AFib amyloidosis) in one or several organs. Renal involvement leading to chronic renal disease and renal failure is a common sign. Additional manifestations depend on the organ involved and the type of amyloid fibrils deposited.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
An unknown % of people have these symptoms.
Click on a symptom to see definitions for associated terms.
|Aplasia of the ulna|
|Dislocated radial head|
|Increased urinary cortisol level|
|Mildly reduced visual acuity|
|Abnormality of orbicularis oris muscle|
|Endopolyploidy on chromosome studies of bone marrow|
|Hypoplastic nasal tip|
|Hypoplastic nasal bridge|
|Autosomal dominant inheritance|
|Generalized amyloid deposition|
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