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.
See also reference (FX) in Slovak
degenerácia makuly
See also reference (FX) in English
Macular Degeneration
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Number of the records: 1
openseadragon
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