Vitelliform Macular Dystrophy

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.

Also Known As:

Adult-Onset Vitelliform Macular Dystrophy; Best Disease; Best Macular Dystrophy; Best Vitelliform Macular Dystrophy; Best's Disease; Foveomacular Dystrophy, Adult-Onset; Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization; Juvenile-Onset Vitelliform Macular Dystrophy; Macular Degeneration, Polymorphic Vitelline; Macular Dystrophy, Vitelliform; Macular Dystrophy, Vitelliform, Adult-Onset; Vitelliform Dystrophy; Vitelliform Macular Dystrophy Type 2; Vitelliform Macular Dystrophy, Adult-Onset; Vitelliform Macular Dystrophy, Early-Onset; Vitelliform Macular Dystrophy, Juvenile-Onset; Adult Onset Vitelliform Macular Dystrophy; Adult-Onset Foveomacular Dystrophies; Adult-Onset Foveomacular Dystrophy; Disease, Best; Disease, Best's; Dystrophies, Adult-Onset Foveomacular; Dystrophies, Vitelliform Macular; Dystrophy, Adult-Onset Foveomacular; Dystrophy, Best Macular; Dystrophy, Vitelliform Macular; Foveomacular Dystrophies, Adult-Onset; Foveomacular Dystrophy, Adult Onset; Juvenile Onset Vitelliform Macular Dystrophy; Macular Dystrophies, Vitelliform; Macular Dystrophy, Best; Vitelliform Macular Dystrophies; Vitelliform Macular Dystrophy, Adult Onset; Vitelliform Macular Dystrophy, Early Onset; Vitelliform Macular Dystrophy, Juvenile Onset

Eye Diseases: 3522
- Retinal Diseases: 3014
  - Retinal Degeneration: 4078
    - Macular Degeneration: 15480
      - Vitelliform Macular Dystrophy: 294
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Vitelliform Macular Dystrophy: 294

E Prieto-Calvo Selected Research

E Prieto-Calvo Research Topics

Disease

Drug/Important Bio-Agent (IBA)