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DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD / BMD) GENE MUTATION Test in Bengaluru

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    Test Recommended For:

    N/A

  • Report Frequency :

    Sample Mon by 11 am; Report Sat

  • view report
  • parameter icon

    Parameters :

    1

  • ₹ 7980
Special Instruction :
Physician prescription is mandatory.

Overview

Duchenne muscular dystrophy (DMD) is an inherited disease that affects only males leading to muscle weakness & wasting. Early signs show delayed ability to sit, stand, walk or speak. It can also affect the heart muscle. DMD is due to a genetic defect which can affect different parts of the body. Becker muscular dystrophy (BMD) is a milder form of the same disease. This test identifies the specific defect in the gene & confirms the diagnosis.

Parameters

Doctor Information

Code

Pre-test Information

Physician prescription is mandatory.

Code

Report Delivery

Sample Mon by 11 am; Report Sat

Code

Code

N116

Category

Category

Genetic disorders

Stability Room

Stability Room

NA

Stability Refrigerated

Stability Refrigerated

72 hrs

Stability Frozen

Stability Frozen

NA

Method

Method

MLPA

Specimen

Usage

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.

Specimen

Specimen

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

Lab Test & Blood Test in Bengaluru

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Key Factors for Consideration

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