Duchenne Muscular Dystrophy (DMD) Carrier Test
This test detects carrier status for Duchenne Muscular Dystrophy in females, identifying if they carry a mutation in the DMD gene.
Duchenne Muscular Dystrophy (DMD) Carrier Test Test in Varanasi Overview
No special preparations needed
- Specimen Source
- Duchenne Muscular Dystrophy (dmd) Carrier Test
The Duchenne Muscular Dystrophy test detects mutations in the DMD gene, responsible for causing progressive muscle weakness and wasting.
Males with a family history of DMD or boys showing delayed motor development, difficulty walking, or frequent falls should undergo this test.
A blood sample is collected for DNA analysis to identify deletions, duplications, or point mutations in the DMD gene.
Positive results confirm a diagnosis of DMD, allowing for early intervention and management.
Patients require multidisciplinary management, including physiotherapy, corticosteroids, and potential gene therapy trials.
Test code
RD1473
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 2 ML |
Specimen stability information
Edta Whole Blood
Collection instructions
Clinical History
Specimen rejection criteria
Test run frequency
Every Day TIME - 10:30
Turn around time
8 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Package price
₹13500
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₹13500