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Nervous system

Location>Home>Nervous system>N001:Neuromuscular


    Genetic testing of Neuromuscular disease is to use the target area capture technology and high-throughput sequencing technology, to detect and analysis the related genes of client's Neuromuscular disease. And in the meantime, it can be in early screening of patients with Neuromuscular disease, as well as to realize individualized medication and specificity of gene therapy to provide important basis for patients through combining with the history, clinical manifestation and information. Mygenostics is aimed to detect and analysis multiple subtypes of Neuromuscular disease by hand in hand with clinical experts, combined with a new generation of high-throughput sequencing technology and bioinformatics analysis, to provide reliable basis for early diagnosis of Neuromuscular patients.
V3-panel covers 14 kinds of hereditary neuromuscular diseases
1 Limb-girdle muscular dystrophy
2 Emery-Dreifuss muscular dystrophy
3 Glycosylation defects caused by congenital muscular dystrophy
4 Myofibrillar myopathy
5 Congenital myopathy
6 Oculopharyngeal muscular dystrophy
7 Distal Myopathy
8 Duchenne Muscular Dystrophy
9 Cardiomyopathy and symptoms of the disease
10 Lipid metabolic disease
11 The disease of sugar and yeast
12 Lipid storage disease
13 glycogen storage disease
14 Other