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Short QT syndrome (SQTS) is an inherited cardiac channelopathy principally caused by defective functioning of both potassium\u2013calcium ion channel that lead to abnormal shortening of QT interval, and an increased risk of ventricular and atrial arrhythmias. Tall T waves in all lead electrocardiogram (ECG), peaked T waves, and narrow\u2010based T waves that are reminiscent of the typical \u201cdesert tent\u201d T waves of hyperkalemia are frequently associated with SQTS. Diagnosis is based on patient's family history, evaluation of symptoms (palpitations and cardiac arrest), and 12\u2010lead ECG. It can be time challenging because of the wide range of QT interval in healthy subjects. Implantable cardioverter defibrillator (ICD) is the first\u2010line therapy in SQTS. Quinidine has the potential to be an effective pharmacological therapy for SQTS patients, especially in young children who are not feasible in ICD implantation, because of the ability to prolong QT interval.<\/jats:p>","DOI":"10.1002\/joa3.12439","type":"journal-article","created":{"date-parts":[[2020,10,6]],"date-time":"2020-10-06T21:20:22Z","timestamp":1602019222000},"page":"962-966","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":55,"title":["Short QT syndrome: The current evidences of diagnosis and management"],"prefix":"10.1002","volume":"36","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1602-3384","authenticated-orcid":false,"given":"Ivana P.","family":"Dewi","sequence":"first","affiliation":[{"name":"Faculty of Medicine Universitas Airlangga Surabaya Indonesia"},{"name":"Faculty of Medicine Duta Wacana Christian University Yogyakarta Indonesia"},{"name":"Department of Cardiology and Vascular Medicine Dr. Soetomo 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