DMD / BMD-79 exons Deletion / Duplication Analysis MLPA Blood(O.S.)

Requirements

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    Sample Required EDTA Blood

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    Preperations Required 3-5 ml of EDTA whole blood required. Clinical/family history, referring clinicians contact number and TRF mandatory.

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    Gender Male & Female

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    Age Group 0 - 99 Years

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    Collection AtHome & Lab

15200
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    1 Observations included

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    Results with in 0 Hours

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DMD / BMD-79 exons Deletion / Duplication Analysis MLPA Blood(O.S.)

Observations Included

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Overview

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. This test is indicated for males with a clinical diagnosis or symptoms of Duchenne or Becker muscular dystrophy and for female relatives.

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