Obstructive Hypertrophic Cardiomyopathy Panel
Obstructive Hypertrophic Cardiomyopathy Panel
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$29.00 USD
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$29.00 USD
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This product is only meant for customers who already purchased a MyGenome Test
Hypertrophic cardiomyopathy typically affects the muscular wall (septum) between the heart's two lower chambers (ventricles). The thickened wall could block blood flow from the heart. This is called obstructive hypertrophic cardiomyopathy.
Obstructive hypertrophic cardiomyopathy (HOCM) is a type of heart disease characterized by the thickening of the heart muscle and the narrowing of the heart's main pumping chamber. Obstructive HOCM is caused by mutations in genes involved in the structure and function of the heart muscle, 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 obstructive HOCM or individuals with symptoms of the condition, such as chest pain, shortness of breath, and dizziness. 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:
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Hypertrophic cardiomyopathy typically affects the muscular wall (septum) between the heart's two lower chambers (ventricles). The thickened wall could block blood flow from the heart. This is called obstructive hypertrophic cardiomyopathy.
Obstructive hypertrophic cardiomyopathy (HOCM) is a type of heart disease characterized by the thickening of the heart muscle and the narrowing of the heart's main pumping chamber. Obstructive HOCM is caused by mutations in genes involved in the structure and function of the heart muscle, 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 obstructive HOCM or individuals with symptoms of the condition, such as chest pain, shortness of breath, and dizziness. 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
- More than 20 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Obstructive Hypertrophic Cardiomyopathy
This product is only meant for customers who already purchased a MyGenome Test
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