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- W2069372899 abstract "Multiple mtDNA deletions have been reported to be a cause of inherited recurrent myoglobinuria. We report a 57-year-old man with autosomal dominant progressive external ophthalmoplegia and multiple mtDNA deletions who developed acute rhabdomyolysis provoked by alcohol. A repeated alcohol intake resulted in a 57-fold increase in serum myoglobin. Patients with mitochondrial myopathy and multiple mtDNA deletions, regardless, of associated phenotype and mode of inheritance, may develop rhabdomyolysis." @default.
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- W2069372899 date "1998-01-01" @default.
- W2069372899 modified "2023-09-27" @default.
- W2069372899 title "Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegia" @default.
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- W2069372899 doi "https://doi.org/10.1212/wnl.50.1.299" @default.
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