Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegia

被引：17

作者：

Melberg, A ^{[1
]}

Holme, E

Oldfors, A

Lundberg, PO

机构：

[1] Univ Uppsala Hosp, Dept Neurol, S-75185 Uppsala, Sweden

[2] Sahlgrens Univ Hosp, Dept Pathol, S-41345 Gothenburg, Sweden

[3] Sahlgrens Univ Hosp, Dept Clin Chem, S-41345 Gothenburg, Sweden

来源：

NEUROLOGY | 1998年 / 50卷 / 01期

关键词：

D O I：

10.1212/WNL.50.1.299

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

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.

引用

页码：299 / 300

页数：2

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