MUSCULAR DYSTROPHY & CONGENITAL MYOPATHY GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited     
This comprehensive gene panel analyzes multiple genes associated with various types of muscular dystrophies and congenital myopathies. These inherited neuromuscular disorders can lead to progressive muscle weakness, delayed motor milestones, respiratory difficulty, and cardiac complications. Early genetic identification helps confirm diagnosis, predict disease severity, guide treatment, and support family counseling. Metropolis Healthcare performs advanced Next-Generation Sequencing (NGS) on EDTA blood to deliver accurate and clinically actionable results that support personalized care

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 17,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. 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 this gene panel test include?
It examines multiple genes linked to muscular dystrophies and congenital myopathies to identify pathogenic or likely pathogenic mutations.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-depth NGS sequencing and expert variant interpretation to ensure precise and reliable genetic findings.

Who should consider taking this test?
Patients with unexplained muscle weakness, delayed motor development, family history of muscle disorders, or suspected neuromuscular disease may benefit.

What sample type is required?
EDTA whole blood is needed for genomic DNA extraction and sequencing.

Is fasting required for this test?
No fasting is necessary for this genetic test.

How can Metropolis Healthcare results help doctors?
Results assist clinicians in confirming diagnosis, guiding treatment plans, evaluating prognosis, and advising genetic counseling.

Can this test detect carrier status?
Yes, it can identify carriers in families with known genetic mutations related to muscular dystrophy or myopathy.

Does Metropolis Healthcare offer follow-up support?
Yes, expert genetic counseling and additional confirmatory testing options are available if required

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