Early Pur Mitochondrial Myopathy In Adult

EMRAH AYTAÇ, HARUN PERU

  • Year : 2011
  • Vol : 27
  • No : 4
  •  Page : 231-232
Mitochondrial disease usually occur as a result at mitochondrial DNA (mtDNA) or nucleer DNA (nDNA) mutations.Findigs in mitochondrial myopathy are often limited with skeletel muscle symptoms, slowly progresive muscle weaknes at extremites and oftalmoplegy due to extaoculer muscle weaknes are common. Muscle weaknes is prominent in the proximal muscles but distal muscle involvement is propable. In this article, we present a patient diagnosed as adult onset mitochondrial myopathy with slow progress in 10 years , regged red fibers in muscle biopsy and ısolated muscle ınvolvement
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
Early Pur Mitochondrial Myopathy In Adult
, Vol. 27 (4)
Received : 18.06.2010, Accepted : 18.06.2010, Published Online : 13.08.2018
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ISSN:1017-6616;
E-ISSN:2149-8059;