- A Case of Congenital Long QT Syndrome Associated with Deafness and Syncope
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Lee SM, Choe CW, Kang HS, Kim KS, Song JS, Bae JH
- KMID: 1858300
- Korean Circ J.
- 1998 Nov;28(11):1882-1888.
- doi: 10.4070/kcj.1998.28.11.1882
Congenital long QT syndrome (LQTS) is an inherited disease characterized by prolonged QT intervals and polymorphic ventricular tachycardia. The clinical manifestations vary from sudden cardiac death by ventricular arrhythmia to... -
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- Large Deletion in KCNQ1 Identified in a Family with Jervell and Lange-Nielsen Syndrome
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Sung JY, Bae EJ, Park S, Kim SY, Hyun YJ, Park SS, Seong MW
- KMID: 1791957
- Ann Lab Med.
- 2014 Sep;34(5):395-398.
- doi: 10.3343/alm.2014.34.5.395
Long QT syndrome (LQTS) is a genetically heterogeneous disorder associated with sequence variations in more than 10 genes; in some cases, it is caused by large deletions or duplications among... -
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- Jervell and Lange-Nielsen Syndrome: Novel Compound Heterozygous Mutations in the KCNQ1 in a Korean Family
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Baek JS, Bae EJ, Lee SY, Park SS, Kim SY, Jung KN, Noh CI
- KMID: 2157860
- J Korean Med Sci.
- 2010 Oct;25(10):1522-1525.
- doi: 10.3346/jkms.2010.25.10.1522
The Jervell and Lange-Nielsen syndrome (JLNS) is an autosomal recessive syndrome characterized by congenital deafness and cardiac phenotype (QT prolongation, ventricular arrhythmias, and sudden death). JLNS has been shown to... -
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- A Case of Congenital Long QT Syndrome with Reccurent Syncope
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Hwang JH, Kim HB
- KMID: 2207575
- J Korean Pediatr Soc.
- 2000 May;43(5):725-729.
Congenital long QT syndrome (LQTS) is a disease characterized by prolongation of ventricle repolarization and by the occurrence, usually during emotional or physical stress, of life-threatening arrhythmias that lead to... -
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