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.
Year introduced: 2011
PubMed search builder options
Subheadings:
Tree Number(s): C11.768.585.439.433, C16.320.290.763
MeSH Unique ID: D057826
Entry Terms:
- 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
Previous Indexing:
See Also: