Rapidly progressive amyloid polyneuropathy associated with a novel variant transthyretin serine 25

被引:0
|
作者
Yazaki, M
Yamashita, T
Kincaid, JC
Scott, JR
Auger, RG
Dyck, PJ
Benson, MD
机构
[1] Indiana Univ, Sch Med, Dept Lab Med & Pathol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Neurol, Indianapolis, IN 46202 USA
[3] Hoosier Neurol, Indianapolis, IN USA
[4] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[5] Richard L Roudebush Vet Affairs Med Ctr, Res Dept, Indianapolis, IN 46202 USA
关键词
amyloidosis; amyloid neuropathy; germline mosaicism; haplotype; transthyretin mutation;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report a 52-year-old woman with a novel transthyretin (TTR) variant serine replacing alanine at residue 25 [Ala25Ser (Serine 25)], who showed a unique clinical picture with a relatively acute onset neuropathy within a few days of an influenza vaccination, progressing to a severe degree within 2 years. Sural nerve biopsy revealed amyloid deposition in the endoneurium. Sequencing of the proband's DNA revealed a G to T transversion at the first position of codon 25 of TTR gene. DNA analysis of this family showed the same mutation in her older sister and a niece, but her parents did not have the mutation. Haplotype analysis revealed the mutation to be clearly linked to haplotype III allele inherited from the proband's father. These results indicate this novel Serine 25 mutation originated in the paternal germline mosaicism. It is possible that the vaccination had an influence on the unique clinical picture, but this remains uncertain, (C) 2002 John Wiley Sons, Inc.
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页码:244 / 250
页数:7
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