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Results 21 - 30 of 68 for Abnormal mitochondria in muscle tissue
  1. HADHA gene 
    ... in tissues and damage the liver, heart, and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/hadha - Genetics
  2. CPT2 gene 
    ... in cells and damage the liver, heart, and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/cpt2 - Genetics
  3. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  4. X chromosome 
    ... without being consciously controlled. In the digestive tract, abnormal layering of these muscles may interfere with peristalsis.Deletions or duplications of ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  5. Autosomal dominant optic atrophy and cataract 
    ... apoptosis).Mutations in the OPA3 gene lead to abnormal mitochondrial function. The mitochondria become misshapen and disorganized and have reduced energy- ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  6. Mitochondrial trifunctional protein deficiency 
    ... build up and damage the liver, heart, and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  7. ACADVL gene 
    ... in tissues and damage the heart, liver, and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/acadvl - Genetics
  8. HADHB gene 
    ... build up and damage the liver, heart, and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/hadhb - Genetics
  9. Ornithine translocase deficiency 
    ... developmental delay, learning disabilities, or stiffness caused by abnormal tensing of the muscles (spasticity). Affected individuals may have chronic liver problems ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  10. Primary coenzyme Q10 deficiency 
    ... muscle tone (hypotonia), involuntary muscle contractions (dystonia), progressive muscle stiffness (spasticity), abnormal eye movements (nystagmus), vision loss caused by degeneration ( ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
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