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Short QT syndrome type 2

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Description

Short QT syndrome is a cardiac channelopathy associated with a predisposition to atrial fibrillation and sudden cardiac death. Patients have a structurally normal heart, but electrocardiography (ECG) exhibits abbreviated QTc (Bazett's corrected QT) intervals of less than 360 ms (summary by Moreno et al., 2015). For a discussion of genetic heterogeneity of short QT syndrome, see SQT1 (609620).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

118

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Genes

External Links

  • OMIM

    609621

  • Orphanet
  • HPO
  • Medgen

    C1865019

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