mitochondrial neurogastrointestinal encephalomyopathy

mitochondrial neurogastrointestinal encephalomyopathy: (MNGIE) a mitochondrial encephalomyopathy of autosomal recessive inheritance, having an onset between the second and fifth decades of life and characterized by intestinal dysmotility, ptosis, cachexia, ophthalmoplegia, peripheral neuropathy, and leukoencephalopathy.

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Mitochondrial neurogastrointestinal encephalopathy syndrome — Classification and external resources ICD 9 277.87 OMIM 603041 … Wikipedia
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