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Successful Pregnancy in a Young Woman with Multiple Acyl-CoA Dehydrogenase Deficiency,acid profile was in the normal range indicating an adequate nutritional support. Pregnancy progressed uneventful and the patient gave birth to a healthy boy without any complication..A careful clinical monitoring associated with an adequate medical/nutritional management may improve pregnancy outcome in women with MADD.coddle 发表于 2025-3-22 00:39:27
Triheptanoin: A Rescue Therapy for Cardiogenic Shock in Carnitine-acylcarnitine Translocase Deficieccessfully treated by triheptanoin. The child was managed, thereafter, on triheptanoin until her death at 3 years of age from a cardiopulmonary arrest in the setting of acute respiratory illness superimposed on chronic hypercarbic respiratory failure.Estrogen 发表于 2025-3-22 06:10:52
Mitochondrial Encephalopathy and Transient 3-Methylglutaconic Aciduria in ECHS1 Deficiency: Long-Teoyl-CoA hydratase, a mitochondrial enzyme encoded by the . gene, was markedly decreased in lymphocytes. Retrospective urine analysis confirms that elevated levels of .-(2-carboxypropyl)cysteamine, .-(2-carboxypropyl)cysteine, and .-acetyl-.-(2-carboxypropyl)cysteine can be a diagnostic clue in the disease spectrum of . mutations.祖先 发表于 2025-3-22 10:25:45
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978-3-662-57576-5Society for the Study of Inborn Errors of Metabolism (SSIEM) 2018杀人 发表于 2025-3-23 00:51:21
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