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214 Possible Causes for Early-Onset Dilated Cardiomyopathy

  • Holiday Heart Syndrome

    An association between the ingestion of acute alcohol and onset of cardiac arrhythmias was first reported in the early 70's.[ncbi.nlm.nih.gov] However, most research has focused on the beneficial effects (the "French paradox") of moderate consumption or the harmful consequences, such as dilated cardiomyopathy, associated[ncbi.nlm.nih.gov]

  • Cardiomyopathy

    cardiomyopathy-1Y AD 23 TRIM63 606131 0 TTN 188840 Tibial muscular dystrophy, tardive; Hereditary myopathy with early respiratory failure; dilated cardiomyopathy type 1G;[centogene.com] […] limb-girdle muscular dystrophy type 2J; early-onset myopathy with fatal cardiomyopathy; familial hypertrophic cardiomyopathy type 9 AD, AR 100 TTR 176300 familial transthyretin[centogene.com] […] amyloidosis AD 13 VCL 193065 dilated cardiomyopathy-1W; Cardiomyopathy, familial hypertrophic, 15 AD 18 The differential diagnosis of hypertrophic cardiomyopathy related[centogene.com]

  • Muscular Dystrophy

    Onset is usually during early adulthood, but may occur as late as the sixth decade. The progression of the disorder is slow.[rarediseases.org] Heart defects including conduction abnormalities and dilated cardiomyopathy may occur. Individuals with this form of LGMD usually remain able to walk.[rarediseases.org]

  • Dilated Cardiomyopathy

    Dilated cardiomyopathy with ataxia syndrome (DCMA) is a rare mitochondrial condition associated with early onset cardiomyopathy and non-progressive ataxia.[ncbi.nlm.nih.gov] […] skeletal and cardiac myopathy, not dominant dilated cardiomyopathy.[doi.org] Supplementary Appendix ); immunohistochemical studies showed that some of these carboxy-terminal truncated titin proteins are integrated into the sarcomere and cause recessive, early-onset[doi.org]

  • Familial Isolated Dilated Cardiomyopathy

    […] with early-onset ventricular dilatation and dysfunction.[nejm.org] cardiomyopathy Familial retinoblastoma Monosomy 13q14 Unilateral retinoblastoma Adult-onset autosomal dominant leukodystrophy Burkitt lymphoma Familial gastric cancer Gastric[csbg.cnb.csic.es] […] disease 1 0 0 Obesity due to leptin receptor gene deficiency Rare endocrine disease 1 1 0 Early-onset autosomal dominant Alzheimer disease Rare neurologic disease 2 0 0 Early-onset[mousebook.org]

  • Dilated Cardiomyopathy Type 2B

    (1.18) 9q34 * Torsion dystonia, early onset - EOTD (16.1) 1q25.2 * LAP1B related muscular dystrophy - (1.9, 1.45) * Limb-Girdle, Muscular dystrophy, type 2Y - LGMD2Y (1.9[195.83.227.65] , with fatal cardiomyopathy (SALMY) (EOMFC) Myosin storage myopathy (MSMA) Naxos disease (NXD) Noonan syndrome 1 (NS1) Noonan syndrome 5 (NS5) Primary dilated cardiomyopathy[ncbi.nlm.nih.gov] […] skeletal and cardiac myopathy, not dominant dilated cardiomyopathy.[nejm.org]

  • Ventricular Tachycardia

    It is noteworthy that genes such as PSEN1 and PSEN2, which are responsible for early-onset Alzheimer disease, have also been implicated in dilated cardiomyopathy.[emedicine.medscape.com]

  • Becker Muscular Dystrophy

    Becker muscular dystrophy (BMD) is a rare cause of dilated cardiomyopathy (DCM).[ncbi.nlm.nih.gov] We present a 23-year-old patient with BMD and early-onset DCM in whom cardiovascular magnetic resonance showed extensive myocardial late gadolinium enhancement and previously[ncbi.nlm.nih.gov]

  • Juvenile Primary Lateral Sclerosis

    […] autosomal dominant Alzheimer disease Familial isolated dilated cardiomyopathy Familial renal cell carcinoma Hereditary chronic pancreatitis Idiopathic bronchiectasis Inclusion[csbg.cnb.csic.es] […] distal myopathy due to VCP mutation Amyotrophic lateral sclerosis Autosomal agammaglobulinemia CLN3 disease Congenital bilateral absence of vas deferens Cystic fibrosis Early-onset[csbg.cnb.csic.es] Progressive non-fluent aphasia Semantic dementia Spinocerebellar ataxia type 15 / 16 Spinocerebellar ataxia type 29 Fibronectin glomerulopathy 22q11.2 deletion syndrome Adult-onset[csbg.cnb.csic.es]

  • Hinman Syndrome

    The onset, severity and progression of dilated cardiomyopathy vary greatly even among members of the same family.[rarediseases.org] Dilated cardiomyopathy can develop during infancy or in early adulthood.[rarediseases.org]

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