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Nervous system

Location>Home>Nervous system>N015:Huntington panel


     Huntington's disease is a single gene autosomal dominant genetic disease. The disease shows extensive degeneration of brain parts, especially in the caudate nucleus atrophy, and is a rare line idiopathic neurodegenerative diseases. The main clinical manifestations are dementia and dance-like movements. Genetic testing of Huntington is to use the target area capture technology and high-throughput sequencing technology, to detect and analysis the related genes of client's Huntington. And in the meantime, it can be in early screening of patients with Huntington, 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 Huntington 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  Huntington patients.

     Huntington's (HTTP), HTTP genes, dynamic mutation and fragment analysis