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.

References in periodicals archive ?

Late-onset familial amyloid polyneuropathy type I (Transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan.

Familial Amyloid Polyneuropathy Type I (Portuguese): Distribution and Characterization of Renal Amyloid Deposits.

Enfermedad renal cronica avanzada en el contexto de polineuropatia amiloidotica familiar tipo I

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