Autosomal dominant hereditary maculopathy with childhood-onset accumulation of LIPOFUSION in RETINAL PIGMENT EPITHELIUM. Affected individuals develop progressive central acuity loss, and distorted vision (METAMORPHOPSIA). It is associated with mutations in bestrophin, a chloride channel.
推出的年份: 2011
副标题
树号: C11.768.585.439.433, C16.320.290.763
MeSH 单一 ID: D057826
进入的组:
Dystrophies, Vitelliform Macular
Dystrophy, Vitelliform Macular
Macular Dystrophies, Vitelliform
Vitelliform Macular Dystrophies
Best Macular Dystrophy
Dystrophy, Best Macular
Macular Dystrophy, Best
Best Vitelliform Macular Dystrophy
Macular Degeneration, Polymorphic Vitelline
Macular Dystrophy, Vitelliform
Vitelliform Dystrophy
Best Disease
Disease, Best
Best's Disease
Disease, Best's
Adult-Onset Vitelliform Macular Dystrophy
Adult Onset Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy, Adult-Onset
Vitelliform Macular Dystrophy, Adult Onset
Macular Dystrophy, Vitelliform, Adult-Onset
Foveomacular Dystrophy, Adult-Onset
Adult-Onset Foveomacular Dystrophies
Adult-Onset Foveomacular Dystrophy
Dystrophies, Adult-Onset Foveomacular
Dystrophy, Adult-Onset Foveomacular
Foveomacular Dystrophies, Adult-Onset
Foveomacular Dystrophy, Adult Onset
Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization
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