MicroreaderTM FMR1 gene detection kit

Fragile X Syndrome (Fragile X Syndrome) is an X-linked genetic disease and one of the most common inherited intellectual disability diseases, second only to Down syndrome in incidence. The cause of the disease is the extended mutation of the FMR1 gene (CGG)n on the X chromosome, which leads to the lack of FMRP protein that maintains normal nerve conduction in the brain. Patients with the disease will have severe mental retardation, developmental delay, language barriers and behavioral problems, including ADHD and autism syndrome, inattention, and accompanied by epilepsy and other symptoms. The kit adopts the three-primer PCR technology recognized by international authoritative guidelines, which can accurately calculate the number of CGG repeats, quickly and accurately distinguish different genotype groups, diagnose patients with fragile X syndrome, and meet the different needs of clinical testing.