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表现为线粒体疾病和自闭症的5q14.3缺失:病例报告

5q14.3 deletion manifesting as mitochondrial disease and autism: case report.

作者信息

Ezugha Herbert, Goldenthal Michael, Valencia Ignacio, Anderson Carol E, Legido Agustin, Marks Harold

机构信息

Sections of Neurology, St Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

J Child Neurol. 2010 Oct;25(10):1232-5. doi: 10.1177/0883073809361165. Epub 2010 Feb 22.

Abstract

Mitochondrial disorders are usually associated with defects of 1 or more of the 5 complexes (I to V) of the electron transport chain, or respiratory chain. Complex I and IV are the 2 most frequent abnormalities of the electron transport chain in humans. The authors report the case of a 12-year-old boy with dysmorphic facies, mental retardation, autism, epilepsy, and leg weakness. Buccal swab electron transport chain analysis revealed severe decrease in complex IV and mild reduction in complex I activity levels. Chromosomal microarray studies, using array-based comparative genomic hybridization, revealed a 1-Mb deletion in the 5q14.3 region. This case illustrates that this deletion can be associated with complex I and IV deficits, hence manifesting as a mitochondrial disease. It could be hypothesized that genes that either encode or regulate the expression and/or assembly of complex IV or I subunits are located within the deleted region of 5q14.3.

摘要

线粒体疾病通常与电子传递链或呼吸链的5种复合物(I至V)中的1种或多种缺陷相关。复合物I和IV是人类电子传递链中最常见的两种异常情况。作者报告了一例12岁男孩的病例,该男孩面容畸形、智力发育迟缓、患有自闭症、癫痫且腿部无力。口腔拭子电子传递链分析显示复合物IV严重减少,复合物I活性水平轻度降低。使用基于阵列的比较基因组杂交技术进行的染色体微阵列研究显示,5q14.3区域存在1兆碱基的缺失。该病例表明,这种缺失可能与复合物I和IV缺陷相关,从而表现为线粒体疾病。可以推测,编码或调节复合物IV或I亚基表达和/或组装的基因位于5q14.3的缺失区域内。

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