학술논문

Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities
Document Type
Article
Source
Amyloid: The Journal of Protein Folding Disorders; December 2002, Vol. 9 Issue: 4 p263-267, 5p
Subject
Language
ISSN
13506129; 17442818
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.