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.