Brachydactyly short stature hypertension (Bilginturan) syndrome: Report on two families

被引:0
|
作者
Chitayat, D
Grix, A
Balfe, JW
Abramowicz, JS
Garza, J
Fong, CT
Silver, MM
Saller, DN
Bresnick, GH
Giedion, A
Lachman, RS
Rimoin, DL
机构
[1] SO CALIF PERMANENTE MED GRP,SACRAMENTO,CA
[2] UNIV ROCHESTER,STRONG MEM HOSP,ROCHESTER,NY 14642
[3] KINDERSPITAL ZURICH,CH-8032 ZURICH,SWITZERLAND
[4] CEDARS SINAI MED CTR,LOS ANGELES,CA 90048
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 73卷 / 03期
关键词
hypertension; short stature; brachydactyly; vasculopathy; intracerebral hemorrhage; autosomal dominant;
D O I
10.1002/(SICI)1096-8628(19971219)73:3<279::AID-AJMG10>3.0.CO;2-G
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on two families with autosomal dominant brachydactyly of hands and feet and hypertension, All affected members of the first family had proportionate short stature, However, the propositus and the affected relatives in the second family were only short compared to unaffected relatives, The hypertension was medically responsive in all cases, The propositus in the second family had poor compliance and a striking generalized vasculopathy. All patients were of normal intelligence and had a normal facial appearance, The brachydactyly-short stature-hypertension syndrome was first reported by Bilginturan et al, [1973] in a Turkish family and the families reported by us are Caucasian and Hispanic, The gene causing this condition in the original Turkish family was recently mapped to 12p, Our report expands our existing knowledge and the ethnic diversity of this syndrome. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:279 / 285
页数:7
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