A De Novo Novel Cardiac Ryanodine Mutation (Ser4155Tyr) Associated with Catecholaminergic Polymorphic Ventricular Tachycardia

We describe the case of a 14‐year‐old girl with a history of syncopal episodes triggered by stress or exercise. Catecholaminergic polymorphic ventricular tachycardia was diagnosed with the aid of an implantable loop recorder. The genetic testing of the patient and her family revealed a de novo novel...

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Detaylı Bibliyografya
Yayımlandı:Ann Noninvasive Electrocardiol
Asıl Yazarlar: Mantziari, Lilian, Vassilikos, Vassilios, Anastasakis, Aris, Kotsaka, Xanthippi, Paraskevaidis, Stelios, Styliadis, Ioannis H, Luria, David
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2013
Konular:
Hereditary Arrhythmia Corner
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6932309/
https://ncbi.nlm.nih.gov/pubmed/24147812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12089
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