Pregnancy and argininosuccinic aciduria

被引：15

作者：

Worthington, S

Christodoulou, J

Wilcken, B

Peat, B

机构：

[1] WESTERN SYDNEY GENET PROGRAM,WESTMEAD,NSW,AUSTRALIA

[2] UNIV SYDNEY,DEPT PAEDIAT & CHILD HLTH,SYDNEY,NSW 2006,AUSTRALIA

[3] ROYAL PRINCE ALFRED HOSP,DEPT PERINATOL,CAMPERDOWN,NSW 2050,AUSTRALIA

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1996年 / 19卷 / 05期

关键词：

D O I：

10.1007/BF01799836

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We present the outcome of a pregnancy in a woman with mild argininosuccinic lyase deficiency to add to the collective experience of the maternal and fetal effects of urea cycle defects. In females affected with argininosuccinic lyase deficiency, careful clinical and biochemical monitoring of pregnancy will minimize the risk of metabolic decompensation in the perinatal period. Furthermore, it would appear that argininosuccinate is not teratogenic to the development of the human fetus.

引用

页码：621 / 623

页数：3

共 9 条

[1] HYPERAMMONEMIA IN WOMEN WITH A MUTATION AT THE ORNITHINE CARBAMOYLTRANSFERASE LOCUS - A CAUSE OF POSTPARTUM COMA [J].