DMD (Duchenne muscular dystrophy)/ BMD (Baker muscular dystrophy) Genetic Detection CapitalBio

Name: DMD (Duchenne muscular dystrophy)/ BMD (Baker muscular dystrophy) Genetic Detection
Brand: CapitalBio Technology Co., Ltd.

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are neuromuscular disorders that primarily affect boys due to an X-linked mutation in the DMD gene, resulting in reduced to near absence of dystrophin or expression of truncated forms of dystrophin. Weakness of the heart and respiratory muscles make this a fatal disorder that requires careful medical management.

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Features of DMD (Duchenne muscular dystrophy)/ BMD (Baker muscular dystrophy) Genetic Detection

The reason you choose CapitalBio DMD/BMD test:

Comprehensive - All exons of DMD gene + upstream and downstream 50bp introns + all known intron pathogenic mutations.
High accuracy - Sequencing depth>500×, accuracy>99.9%.

Application of DMD (Duchenne muscular dystrophy)/ BMD (Baker muscular dystrophy) Genetic Detection

Auxiliary diagnosis: search for the cause of suspected DMD/BMD patients and assist clinical diagnosis.
Fertility guidance: provide fertility guidance for couples who have family history or have given birth to children.
Disease risk assessment: conduct risk assessment for high-risk groups with family history and provide early intervention programs to reduce the risk of disease.

Specification of DMD (Duchenne muscular dystrophy)/ BMD (Baker muscular dystrophy) Genetic Detection

Sample type	Venous Blood/ Dried Blood Spot/Tissue
TAT	20 days

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