Cardiomyopathies Report

Cardiomyopathies

Cardiomyopathies are a group of disorders that affect the heart muscle, leading to abnormal heart function and structure. This report screens for genetic variants associated with various types of cardiomyopathy, including hypertrophic cardiomyopathy, dilated cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy. These conditions can cause symptoms such as chest pain, shortness of breath, and heart palpitations, and can lead to complications such as heart failure and sudden cardiac death.

More than 590 genes analyzed

It is recommended if:

This report is useful for individuals with a family history of cardiomyopathy or sudden cardiac death, or individuals with symptoms such as chest pain, shortness of breath, or heart palpitations. Early diagnosis can inform treatment and management strategies, such as medication, lifestyle changes, or surgical interventions.

List of main conditions:

• Dilated cardiomyopathy
• Hypertrophic cardiomyopathy
• Arrhythmogenic right ventricular cardiomyopathy
• Restrictive cardiomyopathy
• Left ventricular noncompaction cardiomyopathy
• Unclassified cardiomyopathy
• Mixed phenotype cardiomyopathy.