Familial amyloidotic polyneuropathy: report of patients heterozygous for the transthyretin Gly42 gene

Ann Neurol. 1992 Mar;31(3):340-2. doi: 10.1002/ana.410310319.

Abstract

We studied 2 patients from a Japanese family with familial amyloidotic polyneuropathy (FAP). Their clinical features are similar to type 1 FAP, and the proband's rectal tissue contained amyloid that stained with antihuman transthyretin (TTR) antiserum. Direct DNA sequencing of the proband's TTR gene revealed a guanine-for-adenine substitution in the second base of codon 42, producing a glycine for glutamate substitution in the plasma protein.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Amyloid / genetics*
  • Amyloidosis / genetics*
  • Codon
  • DNA Mutational Analysis
  • Genes
  • Heterozygote
  • Humans
  • Male
  • Nervous System Diseases / genetics*
  • Pedigree
  • Prealbumin / genetics*

Substances

  • Amyloid
  • Codon
  • Prealbumin
  • transthyretin, Gly(42)-