⭐ BESTSELLER
🏥 NABL ACCREDITED
MELAS-Mutation Detection
This molecular test detects mitochondrial DNA mutations associated with MELAS syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes). It confirms diagnosis in patients with suggestive neurological and metabolic symptoms. The test is essential for genetic counseling, disease management, and family risk assessment.
8 days
Report Ready
No Fasting
Fasting
5-99
Age Group
Home
Collection
Preparation
Why this test
Fasting Required
Not Required
⏱ Report Time
8 days
🧫 Sample Type
Blood
🎂 Age Group
5-99
👤 Gender
Male,Female
🏠 Collection
Home Visit
MELAS-Mutation Detection
MELAS-Mutation Detection
