eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cardiomyopathy |
| Comorbidity | C0028326|noonan syndrome |
| Sentences | 7 |
| PubMedID- 20450268 | Arrhythmogenic cardiomyopathy in a patient with noonan syndrome. |
| PubMedID- 24382853 | A lethal course of hypertrophic cardiomyopathy in noonan syndrome due to a novel germline mutation in the kras gene: case study. |
| PubMedID- 21269411 | Objectives: to understand relationships and survival implications between structural heart disease and hypertrophic cardiomyopathy in noonan syndrome (noonan syndrome-hcm), we reviewed the clinical course of 138 children with noonan syndrome diagnosed with cardiovascular abnormalities and compared survival with the 30 children with noonan syndrome-hcm with 120 contemporaneous children with nonsyndromic hcm. |
| PubMedID- 22980313 | Background: studies of cardiomyopathy in children with noonan syndrome (ns) have been primarily small case series or cross-sectional studies with small or no comparison groups. |
| PubMedID- 23239527 | Severe hypertrophic cardiomyopathy in noonan syndrome-consider sequencing genes encoding sarcomeric proteins. |
| PubMedID- PMC3944423 | A lethal course of hypertrophic cardiomyopathy in noonan syndrome due to a novel germline mutation in the kras gene: case study. |
| PubMedID- 26380542 | cardiomyopathies in noonan syndrome and the other rasopathies. |
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