Short QT Syndrome Report

Short QT SyndromeShort QT syndrome is a rare genetic disorder that affects the heart's electrical activity. Short QT syndrome is caused by mutations in genes involved in the regulation of ion channels in the heart, and this report tests for genetic variants that are known to affect these processes.5 genes analyzed It is recommended if: This report is designed for individuals with a family history of short QT syndrome or individuals with symptoms of the condition, such as palpitations, syncope, and sudden cardiac arrest. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Short QT Syndrome