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Journal of Rare Cardiovascular Diseases
ISSN: 2299-3711 (Print)
e-ISSN: 2300-5505 (Online)
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31‑year old man with short QT syndrome (RCD code: V‑1A.3)
Sylwia Wiśniowska‑Śmiałek
,  
Paweł Rubiś
,  
Katarzyna Holcman
,  
Barbara Biernac‑Fijałkowskaka‑
,  
Agata Leśniak‑Sobelga
,  
Grzegorz Kopeć Magdalena Kostkiewicz
,  
Piotr Podolec
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Abstract
Short QT (SQTS) syndrome is a rare inherited autosomal dominant cardiac channelopathy associated with malignant ventricular and atrial arrhythmias. It is the severest form of the major channelopathies, with cardiac arrest or sudden cardiac death (SCD) as the most common presentation. We report a case of a young patient in whom ventricular fibrillation was the first manifestation of the disease.
Keywords
rare disease, channelopathy, electrocardiography, implantable cardioverter‑defibrillator
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Keywords
Classification of Rare Cardiovascular Diseases anticoagulation atrial fibrillation atrial septal defect cardiomyopathy computed tomography congenital heart disease echocardiography electrocardiogram electrocardiography heart failure implantable cardioverter‑defibrillator magnetic resonance imaging pregnancy pulmonary arterial hypertension pulmonary hypertension rare cardiovascular disease rare disease right heart catheterization right ventricular failure
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