Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities

Amyloid. 2002 Dec;9(4):263-7. doi: 10.3109/13506120209114104.

Abstract

We report a 45-year-old woman with a new transthyretin (TTR) variant, substitution of leucine for tryptophan at residue 41, who has showed vitreous opacities without any other visceral organ involvement since age of 42. Congo red staining of vitrectomy specimens revealed that the vitreous fluid contained amyloid fibrils, which were strongly positive for immunohistochemical staining using anti-human TTR antiserum. DNA analysis of the TTR gene showed a G to T transversion at the second nucleotide of codon 41, indicating a replacement of tryptophan (TGG) by leucine (TTG). These results indicate that the patient's vitreous amyloid is associated with this novel TTR mutation.

Publication types

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

MeSH terms

  • Amyloidosis / complications
  • Amyloidosis / genetics
  • Amyloidosis / pathology*
  • Base Sequence
  • Eye Diseases / complications*
  • Female
  • Humans
  • Leucine / genetics*
  • Middle Aged
  • Mutation
  • Polymorphism, Restriction Fragment Length
  • Prealbumin / chemistry
  • Prealbumin / genetics*
  • Tryptophan / genetics*
  • Vitreous Body / pathology*

Substances

  • Prealbumin
  • Tryptophan
  • Leucine