MATERNALLY INHERITED CARDIOMYOPATHY BY PCR, EDTA BLOOD

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This test detects genetic mutations associated with maternally inherited cardiomyopathy, a condition affecting heart muscle function and often linked to mitochondrial DNA variants. It helps identify individuals at risk of developing progressive cardiac weakness, arrhythmias, and heart failure. Early genetic diagnosis supports timely treatment planning, family screening, and preventive cardiac monitoring. At Metropolis Healthcare, advanced PCR technology ensures accurate and reliable mutation detection from EDTA blood samples

  • 17 Crores+ Samples Processed
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Price: Rs. 7,350.00

Sample Type: EDTA Blood

Fasting Not Required


Notes: M0051

Frequently Asked Questions (FAQ's):

What does the Maternally Inherited Cardiomyopathy test help diagnose?
It helps detect mitochondrial mutations associated with hereditary cardiomyopathy and related cardiac complications.

How does Metropolis Healthcare perform this genetic test?
Metropolis Healthcare uses highly sensitive PCR-based molecular techniques to analyze DNA for specific disease-causing mutations.

Who should consider taking this test?
Individuals with a family history of cardiomyopathy, unexplained heart failure, arrhythmias, or muscle weakness symptoms.

Why is early testing important?
It enables preventive cardiology assessment, risk evaluation, and timely treatment strategies to avoid severe heart complications.

What sample is required for this test?
EDTA whole blood is collected to isolate DNA for PCR analysis.

Do I need to fast before providing the sample?
No fasting or special preparation is needed.

How long does it take to receive results from Metropolis Healthcare?
Results are usually available in about 10–14 working days depending on genetic complexity.

Can this test assist in family planning and counseling?
Yes, results support genetic counseling and screening for other at-risk family members

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