CARDIAC ABNORMALITIES IN THE BARDET-BIEDL-SYNDROME - ECHOCARDIOGRAPHIC STUDIES OF 22 PATIENTS

被引:79
作者
ELBEDOUR, K
ZUCKER, N
ZALZSTEIN, E
BARKI, Y
CARMI, R
机构
[1] BEN GURION UNIV NEGEV, SOROKA MED CTR, CLIN GENET UNIT, IL-84101 BEER SHEVA, ISRAEL
[2] BEN GURION UNIV NEGEV, SOROKA MED CTR, DIV PEDIAT, IL-84105 BEER SHEVA, ISRAEL
[3] BEN GURION UNIV NEGEV, SOROKA MED CTR, PEDIAT CARDIOL UNIT, IL-84105 BEER SHEVA, ISRAEL
[4] BEN GURION UNIV NEGEV, SOROKA MED CTR, DEPT RADIOL, ULTRASOUND UNIT, IL-84105 BEER SHEVA, ISRAEL
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 52卷 / 02期
关键词
BARDET-BIEDL; HEART; ECHOCARDIOGRAPHY; RENAL;
D O I
10.1002/ajmg.1320520208
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Bardet-Biedl syndrome is an autosomal recessive disorder of polydactyly, obesity, tapetoretinal degeneration, mental retardation, hypogenitalism, and renal involvement. A high incidence of congenital and acquired heart disease was reported in the former ''Laurence-Moon-Biedl-Bardet'' syndrome. However, since the establishment of the Bardet-Biedl syndrome as a separate clinical entity, cardiac involvement has not been evaluated in this disorder. We have performed echocardiographic studies on 22 patients with the Bardet-Biedl syndrome from three extended, highly inbred Bedouin families. In addition to previously reported congenital heart defects we have observed hypertrophy of the interventricular septum and dilated cardiomyopathy. Our findings of cardiac involvement in 50% of the cases suggest that echocardiographic examination should be included in the clinical evaluation and follow-up of patients with Bardet-Biedl syndrome. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:164 / 169
页数:6
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