HYDROMETROCOLPOS FOLLOWING PRENATAL DEXAMETHASONE TREATMENT FOR CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)

被引：13

作者：

COUPER, JJ

HUTSON, JM

WARNE, GL

机构：

[1] ROYAL CHILDRENS HOSP,DEPT ENDOCRINOL & DIABET,PARKVILLE,VIC 3052,AUSTRALIA

[2] ROYAL CHILDRENS HOSP,DEPT GEN SURG,PARKVILLE,VIC 3052,AUSTRALIA

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 1993年 / 152卷 / 01期

关键词：

CONGENITAL ADRENAL HYPERPLASIA; 21-HYDROXYLASE DEFICIENCY; HYDROMETROCOLPOS; DEXAMETHASONE;

D O I：

10.1007/BF02072507

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A female with congenital adrenal hyperplasia (21-hydroxylase deficiency) received prenatal dexamethasone treatment. Suppression of the fetal adrenal was initially inadequate but adequate in later pregnancy. The baby showed masculinisation without clitoral enlargement and a narrow urogenital sinus with resulting hydrometrocolpos. It is possible that dexamethasone treatment which is initially inadequate increases the risk of this latter complication.

引用

页码：9 / 11

页数：3

共 13 条

[1] PRENATAL TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA RESULTING FROM 21-HYDROXYLASE DEFICIENCY [J].