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Results 1 - 6 of 6 for Myopathy with lactic "acidosis," hereditary
  1. Myopathy with deficiency of iron-sulfur cluster assembly enzyme 
    ... ISCU deficiency National Organization for Rare Disorders (NORD) MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY; HML PubMed Drugge U, Holmberg M, Holmgren G, ...
    https://medlineplus.gov/...cy-of-iron-sulfur-cluster-assembly-enzyme - Genetics
  2. Find a Neuromuscular Disease (Muscular Dystrophy Association)  
    Neuromuscular Disorders/Start Here ... Neuromuscular Disorders ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy ...
    https://www.mda.org/disease/list - External Health Links
  3. Neuromuscular Disorders (National Library of Medicine)  
    Neuromuscular disorders affect your neuromuscular system. They can cause problems with: The nerves that control your muscles Your muscles Communication between your ...
    https://medlineplus.gov/neuromusculardisorders.html - Health Topics
  4. MT-ND5 gene 
    ... small percentage of all cases of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). This condition affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy). The MT-ND5 gene variants that cause MELAS ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  5. MT-TH gene 
    ... of people with the features of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) have a mutation in the MT-TH gene. This condition is characterized by recurrent severe headaches, muscle weakness (myopathy), hearing loss, stroke-like episodes including a loss ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  6. Mitochondrial DNA 
    ... can cause the characteristic features of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). Some of these ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics