M0099
MMC (Maternal Myopathy with Cardiomyopathy): Mitochondrial Diseases
Test Details: This assay detects mutations in the mitochondrial DNA which are responsible for maternal inheritance of Myopathies with Cardiomyopathy. Mitochondrial cardiomyopathy can be described as a myocardial condition characterized by abnormal heart-muscle structure, function, or both secondary to genetic defects involving the mitochondrial respiratory chain, in the absence of concomitant coronary artery disease, hypertension, valvular disease or congenital heart disease.
![](assets/img/diagnleftimg.png)
Category
Molecular Genetics
Pre-test Information
Clinical and family history is mandatory.
Report Delivery
4 working days
Gender
All
Organ
Multi-Organ
MMC (Maternal Myopathy with Cardiomyopathy): Mitochondrial Diseases
4400
Most Searched Diagnostic Tests