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DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD / BMD) GENE MUTATION (N116) -Delhi

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DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD / BMD) GENE MUTATION (N116) -Delhi

DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD / BMD) GENE MUTATION (N116) - Delhi

OUTSOURCE

|

Pathology

Also Known As:

Duchenne/Becker Muscular Dystrophy (Dmd/Bmd) Gene Mutation

DMD/BMD Gene Mutation

Duchenne and Becker Muscular Dystrophy (DMD & BMD) are X-linked neuromuscular diseases of childhood resulting from a defect in the dystrophin gene. Deletion of one or more exons in the dystrophin gene may cause DMD/BMD. This assay detects deletions in all 79 exons of the dystrophin gene in both males & females.

  • DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD / BMD) GENE MUTATION

3 mL (2 mL min.) whole blood in 1 lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Physician prescription is mandatory.

  • Home Collection

    Home Collection: Available

  • Reports Available: 8 Days

    • Frequently Asked Questions

    Outsourced test are being done from Dr. Lal Path Lab. Charges and reporting time is same as of Dr. Lal Path Labs.

    Physician prescription is mandatory.

    It confirms the disease, guides treatment, and helps in family planning and therapy decisions.
TAT Policy

The Turnaround Time (TAT) for a test depends on the following factors:

  • Registration date and time
  • Type of scan or test
  • Scan time or sample collection time

Please note that in uncommon circumstances, TAT may be delayed due to the complexity of the test or reasons beyond our control. You will be informed about the estimated TAT at the time of registration or after completion of the test.

₹ 7980

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