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Results 1 - 10 of 15 for Mitochondrial myopathy
  1. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... no family history of MELAS. MELAS MELAS syndrome Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial myopathy, lactic acidosis, stroke-like episode Myopathy, mitochondrial-encephalopathy- ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
  2. ACAD9 deficiency 
    ... I deficiency National ... 2017 Feb 14. Citation on PubMed
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  3. Barth syndrome 
    ... M, Xu Y. The Function of Tafazzin, a Mitochondrial Phospholipid-Lysophospholipid ... Jan 8. Citation on PubMed
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  4. Myoclonic epilepsy with ragged-red fibers 
    ... A, Volpi N, Dotti MT, Federico A. Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel ... EL, Taylor RW, McFarland R. Mutations in the mitochondrial tRNA Ser(AGY) gene ... retinal degeneration, myopathy and epilepsy. Eur J Hum Genet. 2012 Aug; ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  5. Mitochondrial neurogastrointestinal encephalopathy disease 
    ... show signs and symptoms of the condition. MEPOP Mitochondrial myopathy with sensorimotor polyneuropathy, ophthalmoplegia, and pseudo-obstruction Mitochondrial ...
    https://medlineplus.gov/...rogastrointestinal-encephalopathy-disease - Genetics
  6. Kearns-Sayre syndrome 
    ... and respiration-deficient muscle fibers from patients with mitochondrial myopathy. Hum Mol Genet. 1994 Jan;3(1):13-9. doi: 10.1093/hmg/3.1.13. Erratum In: Hum Mol Genet 1994 Apr;3(4):687. Citation ... with single large-scale mitochondrial DNA deletions. J Hum Genet. 2008;53(7): ...
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  7. TK2-related mitochondrial DNA depletion syndrome, myopathic form 
    ... depletion syndrome 2 (myopathic type) MTDPS2 TK2-related mitochondrial DNA depletion myopathy Genetic Testing Registry: Mitochondrial DNA depletion syndrome, myopathic ...
    https://medlineplus.gov/...ial-dna-depletion-syndrome-myopathic-form - Genetics
  8. Mitochondrial complex III deficiency 
    ... infancy but can appear later.The severity of mitochondrial complex III deficiency varies widely among affected individuals. People who are mildly affected tend to have muscle weakness (myopathy) and extreme tiredness (fatigue), particularly during exercise (exercise ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  9. Myoclonic epilepsy myopathy sensory ataxia 
    ... 16. Citation on PubMed Stumpf JD, Copeland WC. Mitochondrial DNA replication and disease: insights from DNA polymerase gamma mutations. Cell Mol Life Sci. 2011 Jan;68(2):219-33. doi: 10.1007/s00018-010-0530-4. Epub 2010 Oct 8. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
  10. Cytochrome c oxidase deficiency 
    ... are mildly affected tend to have muscle weakness (myopathy) and poor muscle tone ... of DNA is known as mitochondrial DNA (mtDNA). Most cases of cytochrome c oxidase ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
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