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21 Possible Causes for XLCM

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  • Duchenne Muscular Dystrophy

    Abstract Dystrophinopathies include Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), X-linked dilated cardiomyopathy (XLCM), and facioscapulohumeral muscular[ncbi.nlm.nih.gov]

  • Danon Disease

    Here we report long-term follow-up of the second family (XLCM-2), for which a DMD mutation was never found.[ncbi.nlm.nih.gov] Abstract X-linked dilated cardiomyopathy (XLCM) was first described in 1987 and associated with dystrophin gene (DMD) mutations a decade later in one of the original two families[ncbi.nlm.nih.gov] We conclude that XLCM may be the presenting sign of Danon disease and, in the presence of familial history of HCM, pre-excitation, skeletal muscle involvement and retinal[ncbi.nlm.nih.gov]

  • Xeroderma Pigmentosum Complementation Group F

    Pyelonephritis XGPT Proteins Xylosylprotein-4-beta-galactosyltransferase XIBV Virus Xiburema Virus XINV Virus Xingu Virus XISHF Heart Xamoterol In Severe Heart Failure [study] XLCM[medicabbreviations.com] […] excess lactate Xenopus laevis extended release extra large X-linked (inheritance) XLA X linked agammaglobulinaemia XLAS X-linked aqueductal stenosis X-linked Alport syndrome XLCM[globalrph.com]

  • Cardiac Dilatation

    […] dystrophy The X linked forms of DCM includes X linked dilated cardiomyopathy and Barth syndrome Caused by mutations in the dystrophin gene X linked dilated cardiomyopathy (XLCM[pathologyoutlines.com]

  • Dilated Cardiomyopathy 1NN

    [from OMIM:302045 ; 2016.03.11] Cellular phenotype and pathology Disease synonyms X-linked dilated cardiomyopathy CMD3B XLCM DMD-associated dilated cardiomyopathy DCM dystrophinopathy[flybase.org]

  • Xeroderma Pigmentosum Complementation Group C

    […] excess lactate Xenopus laevis extended release extra large X-linked (inheritance) XLA X linked agammaglobulinaemia XLAS X-linked aqueductal stenosis X-linked Alport syndrome XLCM[globalrph.com]

  • Aprosencephaly and Cerebellar Dysgenesis

    Congenital Glycerol Kinase Deficiency X-Linked Congenital Recessive Muscle Hypotrophy With Central Nuclei X-Linked Copper Malabsorption X-Linked Dilated Cardiomyopathy (Xlcm[neo-genetics.com]

  • Familial Isolated Arrhythmogenic Right Ventricular Dysplasia

    X-linked cardiomyopathy (XLCM): molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.[link.springer.com] Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy (XLCM). Circulation 1997;95:2434–2440. PubMed CrossRef Google Scholar 18.[link.springer.com]

  • Partington Syndrome

    Congenital Glycerol Kinase Deficiency X-Linked Congenital Recessive Muscle Hypotrophy With Central Nuclei X-Linked Copper Malabsorption X-Linked Dilated Cardiomyopathy (Xlcm[neo-genetics.com]

  • Familial Isolated Dilated Cardiomyopathy

    Linkage of XLCM to the centromeric portion of the dystrophin locus was demonstrated, with a combined maximum lod score of 4.33 (at theta 0.0) using 2-point linkage and 4.81[dmd.nl]

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