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Results 1 - 10 of 16 for Long QT syndrome 5
  1. SCN5A gene 
    ... the most common form of an arrhythmia called long QT syndrome. Mutations in this gene account for five to 10 percent of cases of Romano-Ward ... death. A small percentage of cases of acquired long QT syndrome occur in people who have an underlying ... HH1 LQT3 Nav1.5 SCN5A_HUMAN Sodium channel protein, cardiac muscle alpha- ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  2. Romano-Ward syndrome 
    ... PubMed Central Nakano Y, Shimizu W. Genetics of long-QT syndrome. J Hum Genet. 2016 Jan;61(1):51-5. doi: 10.1038/jhg.2015.74. Epub 2015 ... on PubMed Schwartz PJ, Crotti L, Insolia R. Long-QT syndrome: from ... Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):868-77. doi: 10.1161/CIRCEP.111. ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  3. KCNH2 gene 
    ... CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2. J Arrhythm. 2016 Oct;32(5):373-380. doi: 10.1016/j.joa.2015. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  4. KCNQ1 gene 
    ... Loussouarn G. Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome. Circ Res. 2005 Apr 15;96(7):730- ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  5. Jervell and Lange-Nielsen syndrome 
    ... on PubMed Nakano Y, Shimizu W. Genetics of long-QT syndrome. J Hum Genet. 2016 Jan;61(1):51-5. doi: 10.1038/jhg.2015.74. Epub 2015 ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  6. Timothy syndrome 
    ... on PubMed Marks ML, Trippel DL, Keating MT. Long QT syndrome associated with syndactyly identified in females. Am J Cardiol. 1995 Oct 1;76(10):744-5. doi: 10.1016/s0002-9149(99)80216-1. ...
    https://medlineplus.gov/genetics/condition/timothy-syndrome - Genetics
  7. Andersen-Tawil syndrome 
    ... Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family ... and molecular aspects. Int J Cardiol. 2013 Dec 5;170(1):1-16. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  8. CACNA1C gene 
    ... syndrome is characterized by a heart condition called long QT syndrome, which causes the heart (cardiac) muscle to take ... some cases, people with CACNA1C gene variants have long QT syndrome without the other features of Timothy syndrome. It ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  9. CAV3 gene 
    ... gene have also been identified in people with long QT syndrome, which is a heart condition that causes the ... leading to the abnormal heart rhythm characteristic of long QT syndrome. CAV3_HUMAN caveolin-3 LGMD1C LQT9 M-caveolin ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  10. Short QT syndrome 
    ... Citation on PubMed Gussak I, Bjerregaard P. Short QT syndrome--5 years of progress. J Electrocardiol. 2005 Oct;38(4):375-7. doi: 10.1016/j.jelectrocard.2005.06.012. No abstract available. Citation on PubMed Maluli HA, Meshkov AB. A short story of the short QT syndrome. Cleve Clin J Med. 2013 Jan;80( ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
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