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Ophthalmology and Otohinolaryngology

Location>Home>Ophthalmology and Otohinolaryngology>OT002:Ophthalmic Diseases


    The gene detection of Ophthalmic Diseases uses the target region capture technology and new generation high throughput sequencing technology, to detect and analysis the associated genes in Ophthalmology. It can be early screening in patients with genetic diseases in ophthalmology, combining with the history, clinical manifestations. Mygenostics designed the specific gene acquisition scheme for eye disease to detect the genes mutations by hand in hand with the clinical experts in the field of Ophthalmology, combined with a new generation of high-throughput sequencing technology and advanced bioinformatics analysis. It can be provide a reliable basis for early diagnosis of diseases in ophthalmology according to the individual gene mutation.
Department of Ophthalmology B panel covers 8 major categories of genetic diseases
1 Stargardt Disease
2 Cone-rod dystrophy
3 Blue cone monochromacy
4 Cone dystrophy
5 Retinal cone dystrophy
6 Jalili syndrome
7 Fundus flavimaculatus
8 Retinitis punctata albescens