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Mitochondrial encephalomyopathy — two years follow-up by MRI

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Abstract

A case of mitochondrial encephalomyopathy (MEM) followed-up by MRI for 2 1/2y is presented. MRI showed gross, diffusely distributed white matter lesions in both hemispheres predominantly in frontal, parietal, temporal and occipital locations a marked ventriculomegaly indicative of cerebral atrophy. Except a slight increase of the cerebral atrophy there were no changes in the follow-up examinations. There are no specific MRI findings in MEM, the diagnosis is established by the synopsis of MRI, laboratory data and muscle biopsy.

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Hausegger, K.A., Millner, M.M., Ebner, F. et al. Mitochondrial encephalomyopathy — two years follow-up by MRI. Pediatr Radiol 21, 231–233 (1991). https://doi.org/10.1007/BF02011058

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  • DOI: https://doi.org/10.1007/BF02011058

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