Short QT syndrome

From WikiMD's Wellnesspedia

Short QT syndrome (SQTS) is a rare genetic disorder that affects the heart's electrical system. It is characterized by a shortened QT interval, which can be detected on an electrocardiogram (ECG). This condition can lead to life-threatening arrhythmias and sudden death.

Symptoms[edit | edit source]

The primary symptom of Short QT syndrome is a high risk of sudden, life-threatening arrhythmias. These can lead to syncope, or fainting, and sudden death. Some individuals with SQTS may not exhibit any symptoms until an arrhythmia occurs.

Causes[edit | edit source]

Short QT syndrome is a genetic disorder, caused by mutations in certain genes that regulate the heart's electrical activity. These include the KCNH2, KCNQ1, and KCNJ2 genes. The condition is inherited in an autosomal dominant pattern, meaning an affected individual has a 50% chance of passing the disorder onto their children.

Diagnosis[edit | edit source]

Diagnosis of Short QT syndrome is based on the measurement of the QT interval on an ECG. A QT interval of less than 360 milliseconds is generally considered indicative of SQTS. Genetic testing can also be used to confirm a diagnosis.

Treatment[edit | edit source]

Treatment for Short QT syndrome primarily involves managing the risk of arrhythmias. This can include the use of beta blockers, implantable cardioverter defibrillators (ICDs), and in some cases, surgical procedures.

Prognosis[edit | edit source]

With appropriate management, individuals with Short QT syndrome can lead normal lives. However, the risk of sudden death remains, making regular monitoring and treatment essential.

See also[edit | edit source]

Cardiovascular disease A-Z

Most common cardiac diseases

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Short QT syndrome Resources

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Contributors: Admin, Prab R. Tumpati, MD