OPITZ C-SYNDROME AND PSEUDOHYPOALDOSTERONISM

被引：17

作者：

DEKOSTER, J

LEGIUS, E

DEZEGHER, F

DEVLIEGER, H

FRYNS, JP

EGGERMONT, E

机构：

[1] CATHOLIC UNIV LEUVEN,ZIEKENHIUS GASTHUISBERG,DEPT PEDIAT,HERESTR 49,B-3000 LOUVAIN,BELGIUM

[2] CATHOLIC UNIV LEUVEN,CTR HUMAN GENET,B-3000 LOUVAIN,BELGIUM

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 37卷 / 04期

关键词：

multiple congenital anomalies; rare autosomal recessive conditions; trigonocephaly;

D O I：

10.1002/ajmg.1320370405

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

The C syndrome of multiple congenital anomalies is described in a male infant with pseudohypoaldosteronism. The association of these 2 rare autosomal recessive conditions is discussed.

引用

页码：457 / 459

页数：3

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