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Short QT syndrome
URL of this page: https://medlineplus.gov/genetics/condition/short-qt-syndrome/

Short QT syndrome

Description

Short QT syndrome is a condition that can cause a disruption of the heart's normal rhythm (arrhythmia). In people with this condition, the heart (cardiac) muscle takes less time than usual to recharge between beats. The term "short QT" refers to a specific pattern of heart activity that is detected with an electrocardiogram (EKG), which is a test used to measure the electrical activity of the heart. In people with this condition, the part of the heartbeat known as the QT interval is abnormally short.

If untreated, the arrhythmia associated with short QT syndrome can lead to a variety of signs and symptoms, from dizziness and fainting (syncope) to cardiac arrest and sudden death. These signs and symptoms can occur any time from early infancy to old age. This condition may explain some cases of sudden infant death syndrome (SIDS), which is a major cause of unexplained death in babies younger than 1 year. However, some people with short QT syndrome never experience any health problems associated with the condition.

Frequency

Short QT syndrome appears to be rare. At least 70 cases have been identified worldwide since the condition was discovered in 2000. However, the condition may be underdiagnosed because some affected individuals never experience symptoms.

Causes

Mutations in the KCNH2, KCNJ2, and KCNQ1 genes can cause short QT syndrome. These genes provide instructions for making channels that transport positively charged atoms (ions) of potassium out of cells. In cardiac muscle, these ion channels play critical roles in maintaining the heart's normal rhythm. Mutations in the KCNH2, KCNJ2, or KCNQ1 gene increase the activity of the channels, which enhances the flow of potassium ions across the membrane of cardiac muscle cells. This change in ion transport alters the electrical activity of the heart and can lead to the abnormal heart rhythms characteristic of short QT syndrome.

Some affected individuals do not have an identified mutation in the KCNH2, KCNJ2, or KCNQ1 gene. Changes in other genes that have not been identified may cause the disorder in these cases.

Learn more about the genes associated with Short QT syndrome

  • CACNA1C
  • KCNH2
  • KCNJ2
  • KCNQ1

Inheritance

Short QT syndrome appears to have an autosomal dominant pattern of inheritance, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Some affected individuals have a family history of short QT syndrome or related heart problems and sudden cardiac death. Other cases of short QT syndrome are classified as sporadic and occur in people with no apparent family history of related heart problems.

Other Names for This Condition

  • SQTS

Additional Information & Resources

Genetic Testing Information

  • Genetic Testing Registry: Short QT syndrome type 1 From the National Institutes of Health
  • Genetic Testing Registry: Short QT syndrome type 2 From the National Institutes of Health
  • Genetic Testing Registry: Short QT syndrome type 3 From the National Institutes of Health

Patient Support and Advocacy Resources

  • National Organization for Rare Disorders (NORD)

Clinical Trials

  • ClinicalTrials.gov From the National Institutes of Health

Catalog of Genes and Diseases from OMIM

  • SHORT QT SYNDROME 1; SQT1
  • SHORT QT SYNDROME 2; SQT2
  • SHORT QT SYNDROME 3; SQT3

Scientific Articles on PubMed

  • PubMed From the National Institutes of Health

References

  • Bjerregaard P, Gussak I. Short QT syndrome. Ann Noninvasive Electrocardiol. 2005 Oct;10(4):436-40. doi: 10.1111/j.1542-474X.2005.00064.x. Citation on PubMed
  • Borggrefe M, Wolpert C, Antzelevitch C, Veltmann C, Giustetto C, Gaita F, Schimpf R. Short QT syndrome. Genotype-phenotype correlations. J Electrocardiol. 2005 Oct;38(4 Suppl):75-80. doi: 10.1016/j.jelectrocard.2005.06.009. Citation on PubMed or Free article on PubMed Central
  • Brugada R, Hong K, Cordeiro JM, Dumaine R. Short QT syndrome. CMAJ. 2005 Nov 22;173(11):1349-54. doi: 10.1503/cmaj.050596. Citation on PubMed or Free article on PubMed Central
  • Gaita F, Giustetto C, Bianchi F, Wolpert C, Schimpf R, Riccardi R, Grossi S, Richiardi E, Borggrefe M. Short QT Syndrome: a familial cause of sudden death. Circulation. 2003 Aug 26;108(8):965-70. doi: 10.1161/01.CIR.0000085071.28695.C4. Epub 2003 Aug 18. Citation on PubMed
  • Giustetto C, Schimpf R, Mazzanti A, Scrocco C, Maury P, Anttonen O, Probst V, Blanc JJ, Sbragia P, Dalmasso P, Borggrefe M, Gaita F. Long-term follow-up of patients with short QT syndrome. J Am Coll Cardiol. 2011 Aug 2;58(6):587-95. doi: 10.1016/j.jacc.2011.03.038. Citation on PubMed
  • Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome: proposed diagnostic criteria. J Am Coll Cardiol. 2011 Feb 15;57(7):802-12. doi: 10.1016/j.jacc.2010.09.048. 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(1):41-7. doi: 10.3949/ccjm.80a.12029. Citation on PubMed
  • Patel U, Pavri BB. Short QT syndrome: a review. Cardiol Rev. 2009 Nov-Dec;17(6):300-3. doi: 10.1097/CRD.0b013e3181c07592. Citation on PubMed
  • Schimpf R, Wolpert C, Gaita F, Giustetto C, Borggrefe M. Short QT syndrome. Cardiovasc Res. 2005 Aug 15;67(3):357-66. doi: 10.1016/j.cardiores.2005.03.026. Citation on PubMed
  • Wolpert C, Schimpf R, Veltmann C, Giustetto C, Gaita F, Borggrefe M. Clinical characteristics and treatment of short QT syndrome. Expert Rev Cardiovasc Ther. 2005 Jul;3(4):611-7. doi: 10.1586/14779072.3.4.611. Citation on PubMed
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Related Health Topics

  • Arrhythmia
  • Congenital Heart Defects
  • Genetic Disorders

MEDICAL ENCYCLOPEDIA

  • Arrhythmias
  • Genetics

Related Medical Tests

  • Electrocardiogram

Understanding Genetics

  • What is the prognosis of a genetic condition?
  • How can gene variants affect health and development?
  • What does it mean if a disorder seems to run in my family?
  • What are the different ways a genetic condition can be inherited?
  • How are genetic conditions treated or managed?

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