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Condition report · Cardiovascular

Short QT Syndrome

A rare inherited heart disorder characterized by an abnormally short QT interval on an electrocardiogram, which increases the risk of life-threatening arrhythmias and sudden cardiac death.

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The condition we analyse

Autosomal dominant

A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified

Genes analysed

Also known as

ventricular arrhythmia associated with short QT syndrome

Includes 4 related subtypes ↓
  • short QT syndrome 7
  • short QT syndrome type 1
  • short QT syndrome type 2
  • short QT syndrome type 3
MONDO:0000453Orphanet 51083MedGen 378835

Other cardiovascular conditions

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