Aluoch J R
Trop Geogr Med. 1984 Jun;36(2):115-22.
Through a questionnaire data were collected from 116 patients with sickle cell disease (SCD) in the Netherlands, about two thirds of all the patients with SCD in the country. Sixty-four percent of the patients are of Surinamese origin, 14% come from the Netherlands Antilles, 11% come from Turkey, and 11% from elsewhere. Two thirds of the patients live in Amsterdam and Rotterdam. Sixty-seven were children and 49 were adults. Sickle cell anaemia (SS disease) was found in 74, sickle cell beta thalassaemia (S beta thal) in 18, and sickle cell haemoglobin C(SC)-disease in 24 patients. Clinical features and treatment are discussed and the data are compared with the results of similar studies in other European countries.
通过问卷调查,从荷兰116例镰状细胞病(SCD)患者中收集了数据,约占该国所有SCD患者的三分之二。64%的患者来自苏里南,14%来自荷属安的列斯群岛,11%来自土耳其,11%来自其他地区。三分之二的患者居住在阿姆斯特丹和鹿特丹。67例为儿童,49例为成人。74例患者被诊断为镰状细胞贫血(SS病),18例为镰状细胞β地中海贫血(Sβthal),24例为镰状细胞血红蛋白C(SC)病。文中讨论了临床特征和治疗方法,并将数据与其他欧洲国家的类似研究结果进行了比较。