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DMD&BMD
SKU: MD-NLMA369 Categories: , , , , , , , , Tags: , , , ,

In Stock

DMD&BMD

฿11,655.00

Additional information

Also Known As

Duchenne/Becker Muscular Dystrophy Panel
Specimen

EDTA whole blood 10 ml (minimum 6 ml)
Turnaround Time

42 Days
Test Code

MD-NLMA369
Test Type

Special
Related Tests

Genetic Testing for Muscular Disorders

Tests for large deletions or duplications in the DMD gene, which causes Duchenne or Becker muscular dystrophy, inherited disorders that weaken muscles over time.

Product tags: Duchenne/Becker Muscular Dystrophy Panel, Family History of Genetic Disorders, Gait Problems, Muscle Weakness, Muscular Dystrophy
Diseases: Muscular Dystrophy
Symptoms: Gait Problems, Muscle Weakness
Habits: Family History of Genetic Disorders
Age Groups: Adolescents, Pediatric
Specimens: EDTA Whole Blood
Diagnostic Methods: MLPA (Multiplex Ligation-Dependent Probe Amplification)
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Description

Tests for large deletions or duplications in the DMD gene, which causes Duchenne or Becker muscular dystrophy, inherited disorders that weaken muscles over time.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Duchenne/Becker Muscular Dystrophy Panel
Specimen

EDTA whole blood 10 ml (minimum 6 ml)
Turnaround Time

42 Days
Test Code

MD-NLMA369
Test Type

Special
Related Tests

Genetic Testing for Muscular Disorders

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