CONGENITAL HEART-DISEASE IN THE 48,XXYY SYNDROME

被引：0

作者：

MESCHEDE, D ^{[1
]}

NEKARDA, T ^{[1
]}

KECECIOGLU, D ^{[1
]}

LOSER, H ^{[1
]}

VOGT, J ^{[1
]}

MINY, P ^{[1
]}

HORST, J ^{[1
]}

机构：

[1] UNIV MUNSTER,DIV PEDIAT CARDIOL,D-48149 MUNSTER,GERMANY

来源：

CLINICAL GENETICS | 1995年 / 48卷 / 02期

关键词：

CASE REPORT; HEART DEFECTS; CONGENITAL; PREVALENCE; TETRALOGY OF FALLOT; XXYY KARYOTYPE;

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We report on an infant with severe tetralogy of Fallot, bilateral preauricular pits, and a 48,XXYY chromosomal complement. This case and evidence collected from the literature suggest that congenital heart disease may occur in the 48,XXYY syndrome more frequently than currently appreciated.

引用

页码：100 / 102

页数：3

共 21 条

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