Short QT Syndrome Panel
€29.00
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This product is only meant for customers who already purchased a Dante Genome Test
Short QT syndrome is a condition that can cause a disruption of the normal rhythm of the heart (arrhythmia). In people with this condition, the heart muscle (cardiac) takes less time than usual to recharge between beats.
Short 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 panel tests for genetic variants that are known to affect these processes.
This panel 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.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
Short QT syndrome is a condition that can cause a disruption of the normal rhythm of the heart (arrhythmia). In people with this condition, the heart muscle (cardiac) takes less time than usual to recharge between beats.
Short 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 panel tests for genetic variants that are known to affect these processes.
This panel 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.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- 5 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Short QT Syndrome
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