Kapur S, Higgins J V, Scott-Emuakpor A B, Dolanski E A
Clin Genet. 1980 Jul;18(1):88-90. doi: 10.1111/j.1399-0004.1980.tb01370.x.
A family is described in which half-siblings, a boy and a girl born to unrelated mothers and a phenotypically normal father, were affected with omphalocele. The suggested mode of transmission remains unclear. Prenatal diagnosis to detect an affected fetus should be offered to relatives of omphalocele-affected individuals.
描述了一个家庭,其中同父异母的兄妹,即由无血缘关系的母亲和表型正常的父亲所生的一个男孩和一个女孩,患有脐膨出。其遗传方式尚不清楚。对于脐膨出患者的亲属,应提供产前诊断以检测出受影响的胎儿。