Price:
Rs. 17,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: G0109
Frequently Asked Questions (FAQ's):
What is the Duchenne Muscular Dystrophy Gene Panel?
This NGS-based test evaluates the DMD gene at Metropolis Healthcare to detect mutations linked to Duchenne and Becker muscular dystrophy.
Why is this test needed?
It confirms the genetic cause of progressive muscle weakness and helps differentiate between Duchenne and Becker forms.
Which sample type is used?
EDTA blood is required for DNA extraction and sequencing.
What mutations can this panel detect?
The test identifies deletions, duplications, and single-nucleotide variants in the DMD gene.
Who should consider this test?
Children with delayed motor milestones, persistent muscle weakness, or high creatine kinase levels.
How reliable is the test at Metropolis Healthcare?
Metropolis uses advanced NGS platforms to ensure high sensitivity and accurate variant detection.
Does the test help in treatment planning?
Yes, specific mutation detection can guide eligibility for targeted therapies such as exon-skipping.
Is genetic counselling recommended?
Yes, counselling helps families understand inheritance patterns and recurrence risks