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J Neurol Sci ; 270(1-2): 23-7, 2008 Jul 15.
Article in English | MEDLINE | ID: mdl-18314141

ABSTRACT

Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) is the most common mitochondrial disease due to mitochondrial DNA (mtDNA) mutations. At least 15 distinct mtDNA mutations have been associated with MELAS, and about 80% of the cases are caused by the A3243G tRNA(Leu(UUR)) gene mutation. We report here a novel tRNA(Val) mutation in a 37-year-old woman with manifestations of MELAS, and compare her clinicopathological phenotype with other rare cases associated tRNA(Val) mutations.


Subject(s)
DNA, Mitochondrial/genetics , MELAS Syndrome/genetics , Mutation , RNA, Transfer, Val/genetics , Adult , Brain/pathology , DNA Mutational Analysis/methods , Female , Humans , MELAS Syndrome/pathology , Magnetic Resonance Imaging/methods , Magnetic Resonance Spectroscopy/methods , Muscle, Skeletal/pathology
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