Hypertrophic Cardiomyopathy (HCM) Testing

Early diagnosis. Better outcomes. Safer lives.

Hypertrophic Cardiomyopathy (HCM) is a genetic condition where the heart muscle becomes abnormally thick, making it harder for the heart to pump blood effectively. While some individuals may live symptom-free, others face risks like chest pain, shortness of breath, arrhythmias, or even sudden cardiac arrest—especially during exertion. At Heart Rhythm Partners, we offer comprehensive HCM testing to detect the condition early, assess your risk, and develop a tailored care plan that puts your safety and health first.

What We Offer in HCM Testing:

Detailed family history evaluation to identify genetic risks.
Advanced echocardiography with strain imaging to assess heart muscle thickness and function.
Electrocardiogram (ECG) and Holter monitoring to detect electrical abnormalities or arrhythmias.
Exercise stress testing to evaluate symptoms and risk under exertion.
Cardiac MRI (in collaboration with imaging centers) for high-resolution heart imaging.
Genetic counseling and testing when indicated, especially for first-degree relatives.
Evaluation for obstructive vs. non-obstructive HCM.
Ongoing follow-up and risk stratification over time.

Early Detection

Identify HCM before symptoms appear or complications develop.

Comprehensive Risk Stratification

We assess your risk of arrhythmias, obstruction, and sudden cardiac events.

Family Focused

Support and testing options for relatives who may also carry the condition.

Why It Matters:

HCM is one of the most common inherited heart conditions and a leading cause of sudden cardiac death in young athletes. However, with early and accurate diagnosis, most patients live long, active lives. Our HCM testing program is designed to identify the condition even before symptoms start, helping you take control with proactive care, lifestyle adjustments, and—in high-risk cases—potential interventions to prevent complications.