4.1 Article

5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report

Journal

JOURNAL OF CHILD NEUROLOGY
Volume 25, Issue 10, Pages 1232-1235

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0883073809361165

Keywords

deletion; mitochondrial; microarray; electron transport

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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.

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