cone-rod dystrophy 6

An inherited pigmentary retinopathy (OMIM:601777) characterised by pigment deposits primarily in the macular region that are seen on fundus examination, with early loss of cone photoreceptors followed by rod degeneration. With time, there is a loss of visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision; severe loss of vision occurs earlier than in retinitis pigmentosa.
Molecular pathology
Defects in GUCY2D, which encodes a retina-specific guanylate cyclase, cause cone-rod dystrophy-6.

单词	cone-rod dystrophy 6
释义	cone-rod dystrophy 6 cone-rod dystrophy 6 An inherited pigmentary retinopathy (OMIM:601777) characterised by pigment deposits primarily in the macular region that are seen on fundus examination, with early loss of cone photoreceptors followed by rod degeneration. With time, there is a loss of visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision; severe loss of vision occurs earlier than in retinitis pigmentosa. Molecular pathology Defects in GUCY2D, which encodes a retina-specific guanylate cyclase, cause cone-rod dystrophy-6.
随便看	tyronic tyronism tyropanic acid tyropanoate tyropanoate sodium tyrophagus putrescentiae tyropitta tyro programming language tyros tyrosamine tyrosemiophily tyrosets tyrosil kinase tyrosin tyrosinaemia tyrosinaemia type 1 tyrosinaemia type 2 tyrosinaemia type ii tyrosinase tyrosinase-like tyrosinase negative oculocutaneous albinism tyrosinase-related protein 1 tyrosinase-related protein 2 tyrosine tyrosine 3-hydroxylase