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Results 1 - 10 of 21 for Long QT syndrome 11
  1. 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.2015.11.009. Epub 2016 Jan 22. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  2. ANK2 gene 
    ... B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects. Heart Rhythm. 2005 Nov;2(11):1218-23. doi: 10.1016/j.hrthm.2005. ...
    https://medlineplus.gov/genetics/gene/ank2 - Genetics
  3. Andersen-Tawil syndrome 
    ... 294-297. doi: 10.1016/j.nmd.2016.11.006. Epub 2016 Nov 18. Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  4. Romano-Ward syndrome 
    ... 00715-4. Citation on PubMed Vincent GM. The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adults. Semin Pediatr Neurol. 2005 Mar;12(1):15-24. doi: 10.1016/j.spen.2004.11.008. Citation on PubMed
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  5. Timothy syndrome 
    ... Clericuzio C, Keating M. A new form of long QT syndrome associated with ... 2006 Feb 15 [updated 2021 Feb 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/condition/timothy-syndrome - Genetics
  6. CDKN1C gene 
    ... same coin. Trends Mol Med. 2014 Nov;20(11):614-22. doi: 10.1016/j.molmed.2014.09.001. ... and severe long-QT syndrome due to deletion of the imprinting center 2 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  7. SCN5A gene 
    ... the most common form of an arrhythmia called long QT syndrome. Mutations in this gene account for five to ... induced heart condition, which is known as acquired long QT syndrome, increases the risk of cardiac arrest and sudden ...
    https://medlineplus.gov/genetics/gene/scn5a - 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. Ankyrin-B syndrome 
    ... QT interval, the condition is sometimes classified as long QT syndrome 4. However, because additional heart problems can result from changes in the same gene, long QT syndrome 4 is usually considered part of ankyrin-B ...
    https://medlineplus.gov/genetics/condition/ankyrin-b-syndrome - Genetics
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