First Spanish family with familial amyloidotic polyneuropathy associated to TTR Thr49Ile mutation

Amyloid. 2003 Mar;10(1):34-5. doi: 10.3109/13506120308995255.

Abstract

We present a Spanish patient with familial amyloidotic polyneuropathy associated with the TTR Thr49Ile mutation previously described in a Japanese patient. This is the first report in a Caucasian patient and the second in the literature. Age of onset at 66 and the clinical picture were similar to the Japanese patient: sensorimotor polyneuropathy, digestive autonomic disturbances, cardiomyopathy and loss of weight. The mutation was diagnosed by DNA sequencing and induced mutation restriction analysis.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amyloid Neuropathies, Familial / genetics*
  • Amyloid Neuropathies, Familial / physiopathology
  • Autonomic Nervous System / physiopathology
  • Digestive System / physiopathology
  • Female
  • Humans
  • Isoleucine / genetics
  • Male
  • Polymorphism, Single-Stranded Conformational
  • Prealbumin / genetics*
  • Spain
  • Threonine / genetics
  • White People

Substances

  • Prealbumin
  • Isoleucine
  • Threonine