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575 Possible Causes for Myosin Storage Myopathy

  • Myosin Storage Myopathy

    body myopathy Armel TZ, Leinwand LA.[ghr.nlm.nih.gov] Myosin storage myopathy, also called hyaline body myopathy, is caused by a pathogenic mutation in the MYH7 gene, encoding for the slow/β-cardiac myosin heavy chain.[ncbi.nlm.nih.gov] Entry H00703 Disease Name Myosin storage myopathy; Hyaline body myopathy Description Myosin storage myopathy (MSM), also called hyaline body myopathy, is a rare congenital[genome.jp]

  • Hyaline Body Myopathy

    Entry H00703 Disease Name Myosin storage myopathy; Hyaline body myopathy Description Myosin storage myopathy (MSM), also called hyaline body myopathy, is a rare congenital[genome.jp] Myosin storage myopathy/hyaline body myopathy is a rare congenital myopathy, with less than 30 cases reported in the literature.[ncbi.nlm.nih.gov] Title Other Names: Hyaline body myopathy Categories: This disease is grouped under: Myosinopathies Myosin storage myopathy is an inherited condition that affects the muscles[rarediseases.info.nih.gov]

  • Congenital Fiber-Type Disproportion Myopathy

    […] of congenital fiber type disproportion in early stages and later evolves to myosin storage myopathy.[readbyqxmd.com] A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy. Neuromuscul Disord. 2011;21(4):254-62.[rarediseases.org] myopathy; myosin storage myopathy; and nonspecific myopathic changes Pathophysiology The gene affected in each disease predicts the presentation of disease features.[emedicine.medscape.com]

  • Distal Myopathy Type 3

    Genetically related (allelic) disorders are familial hypertrophic cardiomyopathy 1 and myosin storage myopathy, however, the clinical picture of MPD1 is distinct from that[orpha.net] Other mutations in MYH7 may cause pure cardiomyopathy, myosin storage myopathy or scapuloperoneal myopathy. 8 , 9 2.[nature.com] , Nonaka distal myopathy, Markesbery-Griggs distal myopathy) (see these terms).[orpha.net]

  • Nemaline Myopathy Type 4

    […] in dominant myosin storage myopathy.[journals.lww.com] Organization for Rare Disorders), rare diseases, Myosin storage Myopathy, Myosin storage myopathy - Genetics Home Reference,U.S.[mdahellas.gr] Learn more Other less relevant matches: Low match MYOPATHY, MYOSIN STORAGE, AUTOSOMAL DOMINANT; MSMA Myosin storage myopathy, also known as hyaline body myopathy, is a congenital[mendelian.co]

  • Zebra Body Myopathy

    […] in dominant myosin storage myopathy.[journals.lww.com] Other rare myopathies include autophagic vacuolar myopathy, cap disease, congenital myopathy with arrest of myogenesis, myosin storage (hyaline body) myopathy and zebra body[hellodoktor.com] Myosin storage myopathy associated with a heterozygous missense mutation in MYH7. Ann Neurol 2003;54:494-500. Back to cited text no. 40 41.[bioline.org.br]

  • Tendinitis

    Myopathy, Hyaline Body, Autosomal Recessive Myopathy, Myosin Storage MYOPATHY, SCAPULOHUMEROPERONEAL myositis myositis fibrosa myositis ossificans myostatin-related muscle[rgd.mcw.edu] Myopathy with Lactic Acidosis, Hereditary Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset Myopathy, Granulovacuolar Lobular, with Electrical Myotonia[rgd.mcw.edu] […] tissue disease Muscle Weakness Muscular Hypoplasia, Congenital Universal, of Krabbe Musculoskeletal Pain Myalgia myofascial pain syndrome Myopathic Carnitine Deficiency myopathy[rgd.mcw.edu]

  • Dilated Cardiomyopathy

    KEYWORDS: Dilated cardiomyopathy; MYH7; Myosin storage myopathy[ncbi.nlm.nih.gov] Abstract Myosin storage myopathy (MSM) is a protein aggregate myopathy caused by the accumulation of myosin in muscle fibres and results from MYH7 mutation.[ncbi.nlm.nih.gov]

  • Nemaline Myopathy

    myopathy; myosin storage myopathy; and nonspecific myopathic changes Pathophysiology The gene affected in each disease predicts the presentation of disease features.[emedicine.medscape.com] Myopathies with protein accumulation Nemaline myopathy Myosin storage myopathy Cap disease Reducing body myopathy Myopathies with cores Central core disease Core-rod myopathy[emedicine.medscape.com] MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy. Neuromuscul Disord. 2007 Apr. 17(4):321-9. [Medline].[emedicine.medscape.com]

  • Fibromyalgia

    Myopathy, Hyaline Body, Autosomal Recessive Myopathy, Myosin Storage MYOPATHY, SCAPULOHUMEROPERONEAL myositis myositis fibrosa myositis ossificans myostatin-related muscle[rgd.mcw.edu] Myopathy with Lactic Acidosis, Hereditary Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset Myopathy, Granulovacuolar Lobular, with Electrical Myotonia[rgd.mcw.edu] […] tissue disease Muscle Weakness Muscular Hypoplasia, Congenital Universal, of Krabbe Musculoskeletal Pain Myalgia myofascial pain syndrome Myopathic Carnitine Deficiency myopathy[rgd.mcw.edu]

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