Yoshida T, Adachi-Usami E, Kimura T
Department of Ophthalmology, Chiba University School of Medicine, Japan.
Ophthalmologica. 1995;209(2):101-5. doi: 10.1159/000310590.
We examined three patients with congenital grouped pigmentation of the retina by means of electroretinography, electro-oculography and visually evoked cortical potentials. Two patients were affected bilaterally and 1 had a unilateral condition. Electrophysiological findings were normal in all patients, and no inheritance patterns for the disease were found in any of the patients' histories. Only 5 cases of this disease have been reported in Asian countries in recent years. We believe that our patients contribute to the sample of such cases regarding racial prevalence.
我们通过视网膜电图、眼电图和视觉诱发电位对3例先天性视网膜色素沉着群患者进行了检查。2例患者为双侧受累,1例为单侧患病。所有患者的电生理检查结果均正常,且在任何患者的病史中均未发现该疾病的遗传模式。近年来,亚洲国家仅报道过5例这种疾病。我们认为我们的患者为该病例在种族患病率方面的样本提供了补充。