Long QT Syndrome
Author:
Affiliation:
1. NHO Kagoshima Medical Center
2. Orange Medical and Welfare Center for Severe Motor and Intellectual Disabilities
Publisher
The Japanese Society of Pediatric Cardiology and Cardiac Surgery
Link
https://www.jstage.jst.go.jp/article/jspccs/39/3/39_2023-0015/_pdf
Reference42 articles.
1. 1) Schwartz PJ, Crotti L, Insolia R: Long QT syndrome: From genetics to management. Circ Arrhythm Electrophysiol 2012; 5: 868–877
2. 2) Schwartz PJ, Ackerman MJ, Antzelevitch C, et al: Inherited cardiac arrhythmias. Nat Rev Dis Primers 2020; 6: 58
3. 3) Wilde AAM, Amin AS, Postema PG: Diagnosis, management and therapeutic strategies for congenital long QT syndrome. Heart 2022; 108: 332–338
4. 4) Jervell A, Lange-Nielsen F: Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death. Am Heart J 1957; 54: 59–68
5. 5) Romano C, Gemme G, Pongiglione R: Report on a similar disease but with normal hearing. Clin Ped 1963; 45: 656–683
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