PedAM
Pediatric Disease Annotations & Medicines
| Disease | syncope |
| Symptom | C1720983|channelopathy |
| Sentences | 5 |
| PubMedID- 25819988 | Introduction and objectives: long qt syndrome is an inherited ion channelopathy that leads to syncope and sudden death. |
| PubMedID- 26018045 | Catecholaminergic polymorphic ventricular tachycardia (cpvt) is a highly malignant genetic channelopathy associated with exertional syncope and reproducible polymorphic ventricular tachycardia with exercise. |
| PubMedID- 24795161 | It is for these reasons that the identification of a cardiomyopathy or channelopathy in patients with syncope is crucial. |
| PubMedID- 20920651 | Long qt syndrome (lqts) is a cardiac channelopathy associated with syncope, seizures, and sudden death. |
| PubMedID- 24080067 | Background: the long qt syndrome (lqts) is an inherited cardiac channelopathy associated with syncope and sudden cardiac death due to ventricular arrhythmias. |
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