Management of Ornithine Transcarbamylase Deficiency in Pregnancy

被引:43
作者
Mendez-Figueroa, Hector [1 ]
Lamance, Kerri [2 ]
Sutton, V. Reid [2 ]
Aagaard-Tillery, Kjersti [1 ]
Van den Veyver, Ignatia [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
Pregnancy; OTC deficiency; urea cycle disorder; UREA-CYCLE DISORDERS; COMA;
D O I
10.1055/s-0030-1254240
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ornithine transcarbamylase (OTC) deficiency is the most common enzymatic deficiency in the urea cycle. In catabolic states, such as the intrapartum and immediate postpartum periods, hyperammonemic comas with permanent neurological damage and death can develop. We report six cases of OTC deficiency during pregnancy managed at our institution and review the literature on OTC deficiency during pregnancy. Using the patient database from our Metabolic Clinic, pregnant OTC deficiency carriers were identified. The antenatal, intrapartum, and postpartum periods were analyzed. Corresponding literature was reviewed and an extensive multidisciplinary management plan developed. All six pregnant women had favorable outcomes. No hyperammonemic episodes occurred, and intensive care unit admissions and hemodialysis were not required. Although risk to women with OTC deficiency during the intra- and postpartum period exists, multidisciplinary management and a coherent plan usually result in successful labor, delivery, and postpartum. A comprehensive plan for patients who develop hyperammonemia is recommended.
引用
收藏
页码:775 / 783
页数:9
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