视网膜色素变性(Retinitis Pigmentosa;RP)是一种遗传型式多样的视网膜色素性萎缩,累及全世界人口的0.5%。临床上可通过眼底的特殊改变以及心理物理学和电诊断学的检查来识别。本病也可与其他几种遗传性疾病并存。基础研究指出,尽管本病尚无特异疗法,但可采取某 Retinitis Pigmentosa (RP) is a genetically diverse retinal pigmented atrophy that affects 0.5% of the world’s population. Clinically, it can be identified by special changes in the fundus as well as by psychophysics and electrodiagnosis. The disease can also coexist with several other genetic diseases. Basic research pointed out that although there is no specific treatment of this disease, but can take some