al-Salem M, Ismail L
Ophthalmology Department, Ibn-Sina Hospital, Kuwait, Arabian Gulf.
Ann Trop Paediatr. 1990;10(2):199-202. doi: 10.1080/02724936.1990.11747430.
A complete ophthalmic examination was carried out of 46 Arab children with various forms of sickle cell disease. Mild and infrequent signs in anterior and posterior segments were found, but no cases of sickle cell retinopathy of any kind were detected. These results were compared with the reported findings in black American children of African origin with the same disease. The probable explanations were the high prevalence of fetal haemoglobin in Arab sicklers, the rarity of sickle cell disease among the Arabs and the possible existence of a different gene.
对46名患有各种镰状细胞病的阿拉伯儿童进行了全面的眼科检查。在前节和后节发现了轻微且不常见的体征,但未检测到任何类型的镰状细胞视网膜病变病例。将这些结果与报道的患有相同疾病的非洲裔美国黑人儿童的检查结果进行了比较。可能的解释是阿拉伯镰状细胞病患者中胎儿血红蛋白的高患病率、阿拉伯人中镰状细胞病的罕见性以及可能存在不同的基因。