FAMILIAL OCCURRENCE OF OMPHALOCELE SUGGESTING SEX-LINKED INHERITANCE

被引：27

作者：

HAVALAD, S

NOBLETT, H

SPEIDEL, BD

机构：

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 1979年 / 54卷 / 02期

关键词：

D O I：

10.1136/adc.54.2.142

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

The occurrence of omphalocele in siblings is rare (McKeown et al., 1953; Irving, 1967; Rothemberg and Barnet, 1974; Rott and Truckenbrodt, 1974) and there is only one report of the presence of this malformation in two generations of a family (Osuna and Lindham, 1976). We report a family in which 4 cases of omphalocele occurred in two generations. Only males were affected, suggesting a sex-linked mode of inheritance.

引用

页码：142 / 143

页数：2