Author/Authors :
Hiroyuki Yamamoto، نويسنده , , Kimikazu Yakuhijin، نويسنده , , entaro Kuuhara، نويسنده , , Michael Franci T. Eca?o، نويسنده , , Azua Nagai، نويسنده , , Akira Negi، نويسنده ,
Abstract :
Purpoe
To report a novel homozygou RDH5 gene mutation in a 76-year-old fundu albipunctatu who developed macular atrophy with the diappearance of white dot.
Deign
Obervational cae report.
Method
Direct genomic equencing for RDH5 mutation wa done after complete ophthalmic examination.
Reult
Fundocopy revealed only macular atrophy with notable abence of white dot. A homozygou G490T (Val164Phe) miene RDH5 gene mutation wa detected.
Concluion
Thi i the firt reported long-term cae of fundu albipunctatu demontrating macular atrophy with fading of the typical white dot. Gene tudie may be the only method for ditinguihing fundu albipunctatu from other type of macular atrophy in the elderly.