Early Pur Mitochondrial Myopathy In Adult

EMRAH AYTAÇ, HARUN PERU

  • EMRAH AYTAÇ: ANKARA DIŞKAPI YILDIRIM BEYAZIT E.A.H
  • HARUN PERU: SELÇUK ÜNİVERSİTESİ TIP FAKÜLTESİ
  • Year : 2011
  • Vol : 27
  • Issue : 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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Conflict of interest : Yok
Selcuk Medical Journal
2011, Vol. 27 (4)
ISSN: 1017-6616
E-ISSN: 2149-8059
Received : , Accepted : , Published Online :