Neuromuscular Disorders

Features of Neuromuscular Disorders

CapitalBio Neuromuscular Disorders test detect 1004 genes, including the exon coding region and its upstream and downstream 10bp intron regions. There are 1,314 genetic diseases included in this test, which can be divided into 5 categories: peripheral neuropathy, muscular dystrophy, myopathy, muscular neuropathy, muscular neuropathy, systemic neuropathy.

• Auxiliary diagnosis: looking for the pathogenicity reason of patients with suspected neuromuscular genetic diseases, auxiliary 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.