Literature DB >> 18310979

Mitochondrial encephalomyopathy associated with diabetes mellitus, cataract, and corpus callosum atrophy.

Minoru Oishi1, Kenji Miki, Akihiko Morita, Kazumi Fujioka, Shigeki Aoki, Ichizo Nishino, Ikuya Nonaka, Yu-ichi Goto, Tomohiko Mizutani.   

Abstract

A 44-year-old woman with mitochondrial encephalomyopathy noticed weakness of the lower extremities at the age of 30 years. She also has type 2 diabetes mellitus, posterior subcapsular cataracts in both eyes, and corpus callosum atrophy. Family history showed that a maternal cousin had a myopathy, 3 maternal aunts had diabetes mellitus, and her mother and 2 maternal aunts had cataracts. External ophthalmoplegia, proximal myopathy, and absent deep tendon reflexes were noted. The mitochondrial DNA 3243 point mutation was negative. Muscle biopsy showed ragged-red fibers, cytochrome c oxidase (COX)-positive fibers, and COX-negative fibers.

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Year:  2008        PMID: 18310979     DOI: 10.2169/internalmedicine.47.0579

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  2 in total

Review 1.  [Cerebral CT and MRI in mitchondrial disorders].

Authors:  J Finsterer
Journal:  Nervenarzt       Date:  2009-06       Impact factor: 1.214

2.  Analysis of mitochondrial DNA variations in Indian patients with congenital cataract.

Authors:  Mascarenhas Roshan; Shama Prasada Kabekkodu; Pai H Vijaya; Kamath Manjunath; Jochen Graw; P M Gopinath; Kapeattu Satyamoorthy
Journal:  Mol Vis       Date:  2012-01-24       Impact factor: 2.367

  2 in total

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