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.
Bests makuladystrofi — Bests sjukdom — Bests vitelliforma makuladystrofi — Vitelliform makuladystrofi typ 2
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 — Juvenile-Onset Vitelliform Macular Dystrophy — Juvenile Onset Vitelliform Macular Dystrophy — Vitelliform Macular Dystrophy, Early-Onset — Vitelliform Macular Dystrophy, Early Onset — Vitelliform Macular Dystrophy, Juvenile-Onset — Vitelliform Macular Dystrophy, Juvenile Onset — Vitelliform Macular Dystrophy Type 2