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A case of late-onset MELAS
K G Kimata1, L Gordan, E T Ajax
1Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City 52242-1053, USA.
Abstract:
We describe a 60-year-old man with MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) and discuss the mitochondrial DNA point mutation 3243. A diagnosis of MELAS should be considered in the appropriate clinical setting at any age.
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