Obstructive Hypertrophic Cardiomyopathy Report
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 report tests for genetic variants that are known to affect these processes.
More than 20 genes analyzed
It is recommended if:
This report 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.
List of main conditions:
- Obstructive Hypertrophic Cardiomyopathy
Simple workflow
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Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.
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*Raw data will be available free of charge for the first 30 days after release.
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