Disease | marfan syndrome |
Phenotype | C0007193|dilated cardiomyopathy |
Sentences | 2 |
PubMedID- 21139296 | dilated cardiomyopathy in a patient with marfan syndrome accompanied by chronic type a aortic dissection and right atrial thrombus. |
PubMedID- 22375212 | A diversity of cardiovascular disorders including hypertrophic cardiomyopathy, congenital coronary anomalies, arrhythmogenic right ventricular dysplasia, dilated cardiomyopathy, aortic rupture due to marfan syndrome, myocarditis, valvular disease and electrical disorders (wolff-parkinson-white syndrome, long qt syndrome, brugada syndrome), as well as commotio cordis represent the common causes of scd in young athletes.as the outcome of lethal cardiovascular disorders is not reversible except in few cases, effective measures should be addressed to reduce the burden of sudden cardiac death in young athletes. |
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