Ezugha Herbert, Goldenthal Michael, Valencia Ignacio, Anderson Carol E, Legido Agustin, Marks Harold
Sections of Neurology, St Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA, USA.
J Child Neurol. 2010 Oct;25(10):1232-5. doi: 10.1177/0883073809361165. Epub 2010 Feb 22.
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.
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。