Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids

被引:32
作者
Lipskind, S. [2 ]
Loanzon, S. [3 ]
Simi, E.
Ouyang, D. W. [1 ]
机构
[1] Univ Chicago, Pritzker Sch Med, NorthShore Univ HealthSyst, Dept Obstet & Gynecol,Div Maternal Fetal Med, Evanston, IL 60201 USA
[2] Northwestern Univ, Dept Obstet & Gynecol, Feinberg Sch Med, Evanston, IL USA
[3] St Francis Hosp, Dept Obstet & Gynecol, Evanston, IL USA
关键词
pregnancy; hyperammonemic coma; ornithine transcarbamylase deficiency; corticosteroids; haloperidol; antenatal; UREA CYCLE DISORDERS; DEFICIENCY; PREGNANCY;
D O I
10.1038/jp.2011.23
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Women who are carriers of the ornithine transcarbamylase (OTC) mutation are at risk for developing hyperammonemia during the postpartum period and at times of metabolic stress. We present a unique case of hyperammonemic coma occurring in an OTC mutation carrier during the antepartum period. Multiple factors, including the administration of antenatal corticosteroids, likely precipitated this critical condition. Clinicians should be aware of this life-threatening clinical presentation and be prepared to identify, treat, and prevent hyperammonemia in affected individuals. Journal of Perinatology (2011) 31, 682-684; doi:10.1038/jp.2011.23
引用
收藏
页码:682 / 684
页数:3
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