familial amyloid polyneuropathy type I
familial amyloid polyneuropathy type I
An autosomal dominant form of hereditary amyloidosis that begins in early adulthood with rapidly progressive symmetrical sensorimotor polyneuropathy that quickly leads to incapacity. FAP I is now recognised as a permutation of transthyretin amyloidosis.Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.