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Results 1 - 10 of 10 for Long QT syndrome
  1. ... 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 ...
  2. ... This condition is a form of arrhythmia called long QT syndrome. In people with Romano-Ward syndrome, the heart ... including sudden infant death syndrome (SIDS) and acquired long QT syndrome.SIDS is a major cause of death in ...
  3. ... most common form of a heart condition called long QT syndrome. Mutations in this gene account for approximately 25 ... induced heart condition, which is known as acquired long QT syndrome, increases the risk of cardiac arrest and sudden ...
  4. ... induced heart condition, which is known as acquired long QT syndrome, increases the risk of cardiac arrest and sudden death. A small percentage of cases of acquired long QT syndrome occur in people who have an underlying mutation ...
  5. ... NCBI Gene ClinVar Chiang CE. Congenital and acquired long QT syndrome. Current concepts and management. Cardiol Rev. 2004 Jul- ... PubMed Central Groffen AJ, Bikker H, Christiaans I. Long QT Syndrome Overview. 2003 Feb 20 [updated 2024 Mar 21]. ...
  6. ... 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 ...
  7. ... 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 ...
  8. ... F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 ...
  9. ... Spuler S, Schuelke M. Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy ...
  10. The KCNQ1OT1 gene is located within another gene, KCNQ1. Because the two genes share a region of overlapping DNA, the KCNQ1OT1 gene is also known as KCNQ1 ...