Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Booking Procedure:
- Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
- Sample will be collected by our technician at your address at given slot.
- You can make the payment to the technician at the time of collection
- Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
- Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.
Frequently Asked Questions (FAQ's):
What does the Myotonia Congenita Gene Panel by NGS include?
This panel analyzes major genes responsible for myotonia congenita, using high-depth sequencing at Metropolis Healthcare for reliable mutation detection.
How does Metropolis Healthcare perform this genetic test?
Metropolis Healthcare uses next-generation sequencing (NGS) to identify disease-causing variants with stringent quality checks and expert genomic analysis.
Who should undergo this test?
Individuals with symptoms like muscle stiffness, delayed relaxation, or suspected hereditary myotonia are ideal candidates for testing at Metropolis Healthcare.
Why is NGS preferred for diagnosing myotonia congenita?
NGS provides comprehensive coverage of multiple genes in a single run, allowing Metropolis Healthcare to deliver accurate and timely results.
How should I prepare for this test at Metropolis Healthcare?
No special preparation is needed; a simple EDTA blood sample is sufficient for the analysis.
Can this test confirm whether the condition is inherited?
Yes, the panel helps identify whether the condition follows a dominant or recessive inheritance pattern, with Metropolis Healthcare offering clear genetic insights.
How long does Metropolis Healthcare take to provide results?
Turnaround time typically ranges from a few weeks, depending on sequencing and analysis workflows.
Does Metropolis Healthcare offer genetic counseling based on the results?
Yes, genetic counseling support is available to help patients and families understand the findings and next steps