Successful management of pregnancy with very-long-chain acyl-coenzyme A dehydrogenase deficiency
| Autor: | Hiroko, Yamamoto, Daisuke, Tachibana, Go, Tajima, Yosuke, Shigematsu, Takashi, Hamasaki, Akemi, Tanaka, Masayasu, Koyama |
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| Rok vydání: | 2014 |
| Předmět: |
Delayed Diagnosis
Mitochondrial Diseases Term Birth Pregnancy High-Risk Acyl-CoA Dehydrogenase Long-Chain Infant Newborn Myalgia Combined Modality Therapy Lipid Metabolism Inborn Errors Fatty Acids Monounsaturated Hospitalization Pregnancy Complications Japan Muscular Diseases Pregnancy Prenatal Diagnosis Congenital Bone Marrow Failure Syndromes Humans Female Labor Induced Child Bed Rest |
| Zdroj: | The journal of obstetrics and gynaecology research. 41(7) |
| ISSN: | 1447-0756 |
| Popis: | Very-long-chain acyl-coenzyme A dehydrogenase deficiency (VLCADD) is a rare and life-threatening disease characterized by an enzymatic defect in the fatty acid β-oxidation pathway. A nulliparous woman with VLCADD showed improvements in serum levels of the long-chain acylcarnitine moiety (C14:1) during pregnancy and successfully delivered a healthy infant vaginally. Pregnancy and vaginal delivery can be successfully completed in patients with VLCADD with careful management. |
| Databáze: | OpenAIRE |
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