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902 Possible Causes for 4' EDMD

Did you mean: 4', EDMD

  • Dilated Cardiomyopathy

    muscular dystrophy Fabry disease hypertrophic cardiomyopathy ( HCM ) transthyretin amyloidosis some of these genes on this panel are also associated with other disorders[invitae.com] muscular dystrophy 2 Limb-girdle muscular dystrophy 1B Charcot–Marie–Tooth disease 2B1 LMNB Barraquer–Simons syndrome LEMD3 Buschke–Ollendorff syndrome Osteopoikilosis LBR[en.wikipedia.org] […] arrhythmogenic right ventricular cardiomyopathy ( ARVC ) dilated cardiomyopathy ( DCM ) dystrophinopathies Becker muscular dystrophy ( BMD ) Duchenne muscular dystrophy ( DMD ) Emery-Dreifuss[invitae.com]

  • Emery-Dreifuss Muscular Dystrophy

    Electron microscopy study of muscle biopsies from patients with autosomal-dominant Emery-Dreifuss muscular dystrophy revealed nuclear alterations in about 10% of the preserved[ncbi.nlm.nih.gov] They are caused by mutations in collagen VI (ColVI) genes (COL6A1, COL6A2, and COL6A3) while LMNA mutations cause autosomal dominant Emery-Dreifuss muscular dystrophy.[ncbi.nlm.nih.gov] Emery-Dreifuss muscular dystrophy.[doi.org]

  • Obesity

    Sedentary lifestyles and increased pollution brought about by industrialization pose major challenges to the prevention of both obesity and chronic respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, obstructive sleep apnea and obesity hypoventilation syndrome. Obesity has emerged[…][ncbi.nlm.nih.gov]

  • Autosomal Dominant Emery-Dreifuss Muscular Dystrophy

    dominant Emery-Dreifuss muscular dystrophy.[ncbi.nlm.nih.gov] Electron microscopy study of muscle biopsies from patients with autosomal-dominant Emery-Dreifuss muscular dystrophy revealed nuclear alterations in about 10% of the preserved[ncbi.nlm.nih.gov] OBJECTIVE: The aim of this study was to evaluate the spectrum of muscle involvement on MRI in patients with autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD2) due[ncbi.nlm.nih.gov]

  • Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2

    Dominant Emery-Dreifuss Muscular DystrophyAutosomal Dominant Emery Dreifuss Muscular DystrophyEmery-Dreifuss Muscular Dystrophy, Autosomal DominantEmery Dreifuss[mesh.kib.ki.se] […] type 1B; EDMD2; EMD2; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Emery-Dreifuss muscular dystrophy, autosomal dominant; Hauptmann-Thannhauser muscular dystrophy[informatics.jax.org] [Mutation analysis of a Chinese family with autosomal dominant Emery-Dreifuss muscular dystrophy].[pesquisa.bvsalud.org]

  • Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

    Dominant Emery-Dreifuss Muscular DystrophyAutosomal Dominant Emery Dreifuss Muscular DystrophyEmery-Dreifuss Muscular Dystrophy, Autosomal DominantEmery Dreifuss[mesh.kib.ki.se] , Scapuloperoneal Muscular Dystrophy, Autosomal Dominant Emery-Dreifuss Muscular Dystrophy, Hauptmann Thannhauser Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, Autosomal[ebi.ac.uk] Back to: « Emery-Dreifuss muscular dystrophy Symptoms List: Emery-Dreifuss muscular dystrophy type 3, autosomal recessive Symptoms and clinical features may include: 2 Clinical[familydiagnosis.com]

  • Emery-Dreifuss Muscular Dystrophy Type 1

    Fernández-Álvarez , Autosomal dominant EmeryDreifuss muscular dystrophy: a new family with late diagnosis , Neuromuscular Disorders , 12 , 1 , (19) , (2002) . A.[doi.org] Muscular Dystrophy Autosomal Dominant Emery Dreifuss Muscular Dystrophy Autosomal Recessive Emery Dreifuss Muscular Dystrophy Emery Dreifuss Muscular Dystrophy Emery Dreifuss[decs.bvs.br] Home Emery Dreifuss Muscular Dystrophy Home Emery Dreifuss Muscular Dystrophy Emery Dreifuss Muscular Dystrophy, Emery Dreifuss Syndrome, Scapuloperoneal Muscular Dystrophy[xpertdox.com]

  • Congenital Muscular Dystrophy due to LMNA Mutation

    Autosomal dominant Emery-Dreifuss muscular dystrophy Atypical Werner syndrome Autosomal codominant severe lipodystrophic laminopathy Autosomal dominant limb-girdle muscular[csbg.cnb.csic.es] Disease Ontology Term OMIM Term OMIM Phenotype ID autosomal dominant Emery-Dreifuss muscular dystrophy 2 Emery-Dreifuss muscular dystrophy 2, autosomal dominant 181350 autosomal[zfin.org] There are varied case reports that exist for autosomal dominant Emery-Dreifuss Muscular Dystrophy.[dovemed.com]

  • Muscular Dystrophy

    Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.[web.archive.org] About 65 percent of autosomal dominant Emery-Dreifuss muscular dystrophy cases are caused by new mutations in the LMNA gene and occur in people with no history of the disorder[ghr.nlm.nih.gov] Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet . 1999 Mar. 21(3):285-8. [Medline] .[emedicine.medscape.com]

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1B

    Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat. Genet. ‏[books.google.com] Autosomal dominant Emery-Dreifuss muscular dystrophy Atypical Werner syndrome Autosomal codominant severe lipodystrophic laminopathy Autosomal recessive Emery-Dreifuss muscular[csbg.cnb.csic.es] – 6 ] The skeletal muscle phenotypes of laminopathy, namely autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) and LGMD1B, are overlapping syndromes exhibiting[bmcresnotes.biomedcentral.com]

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