Fabritius H, Lacroix H, Le Corroller Y
Med Trop (Mars). 1981 Mar-Apr;41(2):147-50.
The clinical, hematologic and biochemical study of three children, carriers of the double heterozygotous SN Baltimore hemoglobin from Guadeloupe, have not allowed to detect any typical anomaly and specially no sign of anemia or hemolysis. An iron deficiency of parasitologic origin has only been detected. This absence of pathological symptoms is related to the fact that SN red cells tend to sickle less rapidly than those from persons with sickle cell trait AS.
对来自瓜德罗普岛的三名携带双杂合子SN巴尔的摩血红蛋白的儿童进行的临床、血液学和生化研究,未发现任何典型异常,尤其没有贫血或溶血迹象。仅检测到寄生虫学来源的缺铁。没有病理症状这一情况与SN红细胞比携带镰状细胞性状AS的人红细胞镰变速度更慢这一事实有关。