Foramina parietalia permagna: Report of nine cases in one family

被引：9

作者：

Kutilek, S

Baxova, A

Bayer, M

Leiska, A

Kozlowski, K

机构：

[1] CHARLES UNIV,FAC MED 1,DEPT PAEDIAT,PRAGUE,CZECH REPUBLIC

[2] CHARLES UNIV,FAC MED 1,DEPT MED GENET,PRAGUE,CZECH REPUBLIC

[3] CHARLES UNIV,FAC MED 1,DEPT RADIOL,PRAGUE,CZECH REPUBLIC

[4] ROYAL ALEXANDRA HOSP CHILDREN,DEPT MED IMAGING,SYDNEY,NSW,AUSTRALIA

来源：

JOURNAL OF PAEDIATRICS AND CHILD HEALTH | 1997年 / 33卷 / 02期

关键词：

foramina parietalia permagna;

D O I：

10.1111/j.1440-1754.1997.tb01023.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Nine members of a family with foramina parietalia permagna (FPP), inherited as an autosomal dominant trait are reported. Although usually benign, FPP may be associated with other malformations.

引用

页码：168 / 170

页数：3

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