Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy is usually caused by genetic abnormalities in the heart muscle. These genetic changes lead to the walls of the heart‘s left ventricle becoming thicker than usual.

The thickened walls can become rigid, which reduces the heart‘s ability to fill with and pump blood effectively with each heartbeat.

It can cause:

Thickening of your heart muscle (especially the ventricles or lower heart chambers).
Left ventricular stiffness.
Mitral valve changes.
Cellular changes.

What causes Hypertrophic CardioMyopathy (HCM)?

Genetics: Hypertrophic cardiomyopathy can be inherited from parents and passed on to children, indicating a genetic issue with the heart muscle‘s characteristics. Numerous genes can contribute to this condition, and the type of hypertrophic cardiomyopathy that develops can vary widely within a family. Some individuals with the gene for hypertrophic cardiomyopathy may never show symptoms.

Other Factors: High blood pressure and aging can also contribute to the development of hypertrophic cardiomyopathy. In some cases, the exact cause remains unknown.

Clinical utility:

Accurate Diagnosis: Identifies specific genetic variants associated with heart conditions for precise diagnosis.
Risk Assessment and Prognosis: Detects genetic variants linked to increased cardiovascular risk, enabling early identification and personalized monitoring.
Family Screening and Genetic Counseling: Facilitates screening of family members for risk assessment and enables informed family planning decisions.
Research and Advancements: Contributes to ongoing research on the genetic basis of cardiovascular diseases, leading to new discoveries and advancements.
Personalized Care: Allows tailored interventions and preventive measures based on individual genetic profiles.
Improved Patient Outcomes: Enhances patient care through precise diagnoses and proactive risk management.

MapmyGenome Offerings

MapmyGenome’s Comprehensive Cardiology Panel offers a comprehensive genetic analysis tailored to your cardiovascular health needs. Our offerings include:

Complete Gene Panel Analysis: We analyze a wide array of genes associated with cardiovascular diseases, ensuring that no significant genetic factors are overlooked.
Detailed Report and Interpretation: Each panel comes with a detailed report that includes an interpretation of the genetic variants found, their clinical significance, and personalized recommendations for management and care.
Genetic Counseling: We provide access to genetic counselors who can help you understand your results, discuss the implications for your health, and assist with any necessary lifestyle or treatment changes.
Family Screening Options: For those concerned about hereditary risks, we offer family screening packages that allow you to assess the cardiovascular risk for your loved ones.
Ongoing Support: Cardiovascular health is a lifelong journey. MapmyGenome provides ongoing support to help you manage your heart health effectively, including updates on the latest research and recommendations based on your genetic profile.