Joishy S K, Hassan K, Lopes M, Lie-Injo L E
Division of Hematology, Kuala Lumpur, Malaysia.
Trans R Soc Trop Med Hyg. 1988;82(4):515-9. doi: 10.1016/0035-9203(88)90489-0.
Clinical studies were carried out on mild Indian sickle cell anaemia in Malaysia, and genetic and fertility studies were carried out on 101 families with and without sickle-cell haemoglobin (Hb S). The Indian sickle cell anaemia patients reached adulthood, and pregnancies and deliveries were uneventful without blood transfusion. There was no foetal wastage and the number of children produced was not significantly different from that in families without Hb S. 28 Indian patients hospitalized with Plasmodium falciparum malaria infection were also examined for their beta S genotype. P. falciparum malaria infection occurred much more frequently in individuals without Hb S than in Hb S carriers.
在马来西亚对轻度印度镰状细胞贫血进行了临床研究,并对101个有和没有镰状细胞血红蛋白(Hb S)的家庭进行了遗传和生育研究。印度镰状细胞贫血患者成年后,妊娠和分娩顺利,无需输血。没有胎儿流产情况,所生育子女的数量与没有Hb S的家庭相比没有显著差异。还对28名因感染恶性疟原虫而住院的印度患者进行了β S基因型检测。恶性疟原虫感染在没有Hb S的个体中比在Hb S携带者中更为常见。