PedAM
Pediatric Disease Annotations & Medicines
| Disease | myocarditis |
| Phenotype | C0007193|dilated cardiomyopathy |
| Sentences | 16 |
| PubMedID- 23775037 | By contrast, idiopathic dilated cardiomyopathy was associated with myocarditis in a quarter of the cases, none of whom had acute disease. |
| PubMedID- 22032061 | We report the case of a young female patient with recent diagnosis of heart failure (dilated cardiomyopathy due to viral myocarditis), who developed angioedema of the small intestine three weeks after initiating treatment with lisinopril. |
| PubMedID- 23977238 | In vivo delivery of adenoviral vector containing interleukin-17 receptor a reduces cardiac remodeling and improves myocardial function in viral myocarditis leading to dilated cardiomyopathy. |
| PubMedID- 23460527 | Immune-mediated myocarditis can lead to dilated cardiomyopathy (dcm) in about one third of the cases, and represents a frequent cause of cardiac failure particularly in young adults (schultheiss et al, 2011). |
| PubMedID- 19578074 | Protein degradation systems in viral myocarditis leading to dilated cardiomyopathy. |
| PubMedID- 21063523 | The possibility of a viral myocarditis with dilated cardiomyopathy as sequelae can not be entirely ruled out, though it is unlikely as there was no acute episode at onset of symptoms and the symptoms were progressive and developed insidiously. |
| PubMedID- 25802766 | myocarditis leading to severe dilated cardiomyopathy in a patient with dengue fever. |
| PubMedID- 20833772 | Background: myocarditis is a cause of a new-onset dilated cardiomyopathy phenotype in children, with small studies reporting high rates of recovery of left ventricular (lv) function. |
| 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. |
| PubMedID- 21111118 | There is particular attention to the relationship of myocarditis with dilated cardiomyopathy. |
| PubMedID- 22328321 | Autoimmunity against m(2)muscarinic acetylcholine receptor induces myocarditis and leads to a dilated cardiomyopathy-like phenotype. |
| PubMedID- 21954874 | Seven consecutive patients were seen in this period: four toddlers (three suffering from fulminant myocarditis and one with dilated cardiomyopathy associated with spongy myocardium) and three adolescents (two with postmyocarditis cardiomyopathy and one with hypertrophic cardiomyopathy and severe restrictive dysfunction after an ischemic event with cardiopulmonary resuscitation [stunned heart]). |
| PubMedID- 26194549 | myocarditis-a frequent cause of dilated cardiomyopathy and sudden cardiac death-typically results from cardiotropic viral infection followed by active inflammatory destruction of the myocardium. |
| PubMedID- 24381086 | Chronic myocarditis can lead to dilated cardiomyopathy (dcm). |
| PubMedID- 24602216 | They are divided into 6 serotypes (cvb1-6) and are the major pathogens of human viral myocarditis that can lead to dilated cardiomyopathy and cardiac failure [66]. |
| PubMedID- 23389951 | Cvbs are the major pathogens of human viral myocarditis that can lead to dilated cardiomyopathy and cardiac failure (27–30). |
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