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Nervous system

Location>Home>Nervous system>N019:Fragile X syndrome


    Fragile X syndrome is caused by the mutation of the formation of the X chromosome in humans. In a period of X chromosome DNA, because the relationship of genetic, it changes sometimes. One is completely changed, and the other is DNA hypermethylation. Genetic testing of Fragile X syndrome is to use the target area capture technology and high-throughput sequencing technology, to detect and analysis the related genes of client's Fragile X syndrome. And in the meantime, it can be in early screening of patients with Fragile X syndrome, 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 Fragile X syndrome 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 Fragile X syndrome patients.

      Fragile X syndrome:FRM1gene CCG repeats detection