This test detects genetic mutations associated with MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes) using PCR technology on EDTA blood. MELAS is a progressive mitochondrial disorder that affects the brain, muscles, and other organs. Early genetic confirmation helps in diagnosis, clinical management, and family counseling. The test identifies specific mitochondrial DNA mutations, most commonly the m.3243A>G variant. Results assist in planning supportive therapies and evaluating risk in family members.
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Price:
Rs. 6,300.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: M0024
Frequently Asked Questions (FAQ's):
What is the purpose of this test?
To confirm the presence of MELAS-associated mitochondrial mutations for diagnosis and management.
Which sample is required?
Whole blood collected in an EDTA tube.
Who should undergo this test?
Individuals with unexplained neurological symptoms, stroke-like episodes, muscle weakness, seizures, or a family history of mitochondrial disorders.
How are results used?
To guide treatment decisions and offer genetic counseling for affected families.
Is fasting required?
No fasting is needed for this test