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Results 1 - 10 of 14 for myosin myopathy
  1. Myosin storage myopathy 
    Myosin storage myopathy is a condition that causes muscle weakness (myopathy) that does not worsen or worsens very slowly ... certain muscle fibers. The signs and symptoms of myosin storage myopathy usually become noticeable in childhood, although they can ...
    https://medlineplus.gov/genetics/condition/myosin-storage-myopathy - Genetics
  2. MYH7 gene 
    ... Free article on PubMed Central Oldfors A. Hereditary myosin myopathies. Neuromuscul Disord. 2007 May;17(5):355-67. ... Cenacchi G, Angelini C. MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy. Neuromuscul Disord. 2007 Apr; ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  3. Freeman-Sheldon syndrome 
    ... heavy-chain mutations cause distal arthrogryposis and developmental myosin myopathy that persists postnatally. Arch Neurol. 2008 Aug;65(8):1083-90. doi: 10.1001/archneur.65.8.1083. Erratum In: Arch Neurol. 2008 ... in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and ...
    https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome - Genetics
  4. MYH3 gene 
    ... heavy-chain mutations cause distal arthrogryposis and developmental myosin myopathy that persists postnatally. Arch Neurol. 2008 Aug;65( ...
    https://medlineplus.gov/genetics/gene/myh3 - Genetics
  5. Congenital fiber-type disproportion 
    ... MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy. Neuromuscul Disord. 2011 Apr;21(4):254-62. ...
    https://medlineplus.gov/.../congenital-fiber-type-disproportion - Genetics
  6. Laing distal myopathy 
    ... Rozemuller A, Laing NG. Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy. J ... NG. Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1). Am J Hum Genet. 2004 Oct;75( ...
    https://medlineplus.gov/genetics/condition/laing-distal-myopathy - Genetics
  7. TPM3 gene 
    ... researchers suggest they may interfere with normal actin-myosin binding, impairing muscle contraction and resulting in the muscle weakness that occurs in cap myopathy. More About This Health Condition At least 10 ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  8. TPM2 gene 
    ... researchers suggest they may interfere with normal actin-myosin binding, impairing muscle contraction and resulting in the muscle weakness that occurs in cap myopathy. More About This Health Condition At least three ...
    https://medlineplus.gov/genetics/gene/tpm2 - Genetics
  9. Cap myopathy 
    ... researchers suggest they may interfere with normal actin-myosin binding between the thin and thick filaments, impairing muscle contraction and resulting in the muscle weakness that occurs in cap myopathy. ACTA1 TPM2 TPM3 Cap myopathy is an autosomal ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
  10. Intranuclear rod myopathy 
    ... thick filaments made up of another protein called myosin are the primary ... intranuclear rod myopathy result in the accumulation of rods of skeletal ...
    https://medlineplus.gov/genetics/condition/intranuclear-rod-myopathy - Genetics
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