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脂肪酸氧化障碍:母体健康与新生儿结局。

Fatty acid oxidation disorders: maternal health and neonatal outcomes.

机构信息

Division of Gastroenterology and Hepatology, University of Missouri-Columbia, Columbia, Missouri 65212, USA.

出版信息

Semin Fetal Neonatal Med. 2010 Jun;15(3):122-8. doi: 10.1016/j.siny.2009.10.006. Epub 2009 Nov 17.

Abstract

Mitochondrial fatty acid beta-oxidation (FAO) disorders have become an important group of inherited metabolic disorders causing serious pediatric and maternal morbidity and mortality. More than 20 defects affecting beta-oxidation have been discovered, characterized by distinct enzyme or transporter deficiencies. This growing number of FAO disorders covers a wide spectrum of phenotypes and are characterized by a wide array of clinical presentations. We discuss the major mitochondrial FAO disorders and the impact they have on maternal health and neonatal outcomes; diagnostic tools and the value of genetic screening are reviewed; and current therapeutic approaches and management strategies are discussed.

摘要

线粒体脂肪酸β氧化(FAO)障碍已成为导致严重儿科和孕产妇发病率和死亡率的一类重要遗传性代谢紊乱。已经发现了 20 多种影响β氧化的缺陷,其特征为不同的酶或转运蛋白缺乏。越来越多的 FAO 障碍涵盖了广泛的表型,并具有广泛的临床表现。我们讨论了主要的线粒体 FAO 障碍及其对孕产妇健康和新生儿结局的影响;回顾了诊断工具和遗传筛查的价值;并讨论了当前的治疗方法和管理策略。

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