Peripartum management of two parturients with ornithine transcarbamylase deficiency
Author:
Publisher
Elsevier BV
Subject
Anesthesiology and Pain Medicine,Obstetrics and Gynaecology
Reference21 articles.
1. Urea cycle disorders: diagnosis, pathophysiology, and therapy;Brusilow;Adv Pediatr,1996
2. Ornithine transcarbamylase deficiency: a urea cycle defect;Gordon;Eur J Paediatr Neurol,2003
3. Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic coma;Gaspari;Ann Emerg Med,2003
4. Neurological outcome of patients with ornithine carbamoyltransferase deficiency;Nicolaides;Arch Dis Child,2002
5. Late diagnosis of ornithine transcarbamylase defect in three related female patients: polymorphic presentations;Legras;Crit Care Med,2002
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1. Two pregnancies of an ornithine carbamoyltransferase deficiency disease carrier and review of the literature;Nutrición Hospitalaria;2024
2. The management and clinical outcomes of pregnancies in women with urea cycle disorders: A review of the literature and results of an international survey;Journal of Inherited Metabolic Disease;2023-12-09
3. Considerations for prenatal and postpartum management of a female patient with ornithine transcarbamylase deficiency;Molecular Genetics and Metabolism Reports;2022-12
4. Ornithine transcarbamylase deficiency and pregnancy: A case series and review of recommendations;Case Reports in Women's Health;2022-04
5. Effect of Ornithine Transcarbamylase (OTC) Deficiency on Pregnancy and Puerperium;Diagnostics;2022-02-05
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