eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | left ventricular noncompaction |
| Symptom | C0878544|cardiomyopathy |
| Sentences | 4 |
| PubMedID- 25335496 | In contrast to heterozygous pathogenic mutations, homozygous or compound heterozygous truncating pathogenic mybpc3 mutations cause severe neonatal cardiomyopathy with features of left ventricular noncompaction and septal defects in approximately 60% of patients. |
| PubMedID- 21095364 | Here we report an extremely rare case of surgery in a patient with arrhythmogenic left ventricular cardiomyopathy associated with left ventricular noncompaction. |
| PubMedID- 24268868 | The authors present a rare case of hypertrophic cardiomyopathy associated with left ventricular noncompaction cardiomyopathy and coronary artery-left ventricular fistulae in a 42-year-old woman presenting with non-st-elevation myocardial infarction. |
| PubMedID- 24046479 | Peripartum cardiomyopathy associated with left ventricular noncompaction phenotype and reversible rigid body rotation. |
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