Familial digital arthropathy-brachydactyly

被引:9
作者
Amor, DJ
Tudball, C
Gardner, RJM
Lamandé, SR
Bateman, JF
Savarirayan, R
机构
[1] Royal Childrens Hosp, Genet Hlth Serv Victoria, Parkville, Vic 3052, Australia
[2] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[3] Gippsland Base Hosp, Dept Radiol, Sale, Vic, Australia
[4] Univ Melbourne, Dept Radiol, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Dept Paediat, Cell & Matrix Biol Res Unit, Parkville, Vic 3052, Australia
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 108卷 / 03期
关键词
digital arthropathy; brachydactyly; skeletal dysplasia; arthritis; autosomal dominant;
D O I
10.1002/ajmg.10269
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
We report a large family with a previously undescribed, dominantly inherited condition comprising arthropathy of the hands and feet and progressive shortening of the middle and distal phalanges. We have designated the condition familial digital arthropathy-brachydactyly (FDAB). Onset of FDAB is in the first decade and the arthropathy is progressive, resulting in deformity and pain in adult life. The remainder of the skeleton is not affected. It is hypothesized from the radiological appearance of patients at different ages that FDAB might result from subehondral pathology primarily affecting the heads of the phalanges, metacarpals, and metatarsals, with the arthropathy and brachydactyly being secondary effects. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:235 / 240
页数:6
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