eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cardiomyopathy |
| Symptom | C1839611|n syndrome |
| Sentences | 13 |
| PubMedID- 20450268 | Arrhythmogenic cardiomyopathy in a patient with noonan syndrome. |
| PubMedID- 26042521 | Background: mild intrinsic cardiomyopathy in patients with marfan syndrome (mfs) has consistently been evidenced by independent research groups. |
| 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 | Survival implications: hypertrophic cardiomyopathy in noonan syndrome. |
| PubMedID- 25755184 | Objectives: this report aims to evaluate the existence of primary and secondary cardiomyopathy in patients with marfan syndrome (mfs) who underwent surgical management for primary cardiovascular sequelae of this genetic disorder. |
| PubMedID- 21139296 | Dilated cardiomyopathy in a patient with marfan syndrome accompanied by chronic type a aortic dissection and right atrial thrombus. |
| PubMedID- PMC3944423 | A lethal course of hypertrophic cardiomyopathy in noonan syndrome due to a novel germline mutation in the kras gene: case study. |
| PubMedID- 24680252 | First description of arrhythmogenic right ventricular cardiomyopathy in a patient with down syndrome. |
| 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- 20622352 | A case of sheehan syndrome with dilated cardiomyopathy is presented in whom hormone replacement with levothyroxine and prednisolone resulted in complete recovery of cardiomyopathy. |
| PubMedID- 24531548 | Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with marfan syndrome. |
| PubMedID- 24032295 | Dilated cardiomyopathy in a patient with 22q11.2 microdeletion syndrome. |
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