HCM can range from mild to serious. Many people live normal lives with few or no symptoms. However, in some cases, it can lead to complications like irregular heart rhythms or heart failure. Regular follow-up with specialists helps keep it under control.
Some people have symptoms like chest pain, shortness of breath, or palpitations. Others may not feel anything. HCM is often diagnosed using tests like an echocardiogram (heart ultrasound), ECG, or MRI. If a family member has HCM, you should get checked even if you feel fine.
Yes. HCM can affect people at any age, including children. If HCM runs in the family, children should be screened regularly starting in their early teens—or earlier if symptoms appear.
There is no cure yet, but there are excellent treatments. Many people manage their symptoms with medication, and some may need procedures like an implantable defibrillator (ICD) or septal reduction therapy. With proper care, most patients live full and active lives.
That depends on your condition. Some activities may be safe, while others (especially competitive or high-intensity sports) could be risky. Our team can help you create a safe and healthy exercise plan.
Your physician will decide if your family members should be tested. HCM is often inherited, so first-degree relatives (parents, siblings, children) may need to be screened regularly, even if they have no symptoms.
Genetic testing can help confirm the diagnosis and identify who else in your family may be at risk. It’s optional but recommended in many cases. Our center offers counseling to help you understand the process and what the results mean.
If you or a loved one has been diagnosed with HCM or if heart disease runs in your family we’re here to help.