CentoVision
378 genaCentoVision panel (378 gena) je pažljivo dizajniran da bi se otkrili genetski uzroci bolesti oka, uključujući i one koji dovode do sljepila kod novorođenčadi, djece i odraslih. Podrazumijeva najčešće oftalmološke bolesti kao što su, urođeni glaukom, retinitis pigmentosa, strgardt - ova bolest, Stickler sindrom, ahromatopsija i Usher sindrom. Takođe ispituje i različite tipove albinizma.
Subpaneli
- Achromatopsia panel
- Albinism panel
- Bardet-Biedl panel
- Cataract panel
- Cone-rod and cone dystrophy panel
- Flecked retina panel
- Glaucoma panel
- Hermansky-Pudlak syndrome panel
- Leber congenital amaurosis panel
- Meckel syndrome panel
- Microphthalmia/anophthalmia/coloboma spectrum panel
- Oculomotor apraxia panel
- Ophthalmoplegia progressive external panel
- Optic atrophy panel
- Retinitis pigmentosa panel, autosomal dominant
- Retinitis pigmentosa panel, autosomal recessive
- Stargardt disease panel
- Stickler syndrome panel
- Usher syndrome panel
- Vitreoretinopathy and Wagner syndrome panel