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Boosting services for people with sickle-cell disease

机译:增强针对镰状细胞病患者的服务

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The Igbo people of Nigeria called them Ogbanje-malevolent children destined to be lazy and die and be reborn repeatedly. Particular families were plagued by such children who usually died before their 10th birthday. Belief in Ogbanje is centuries old, but a little more than 100 years ago, a less ethereal explanation for the Ogbanje was found. Walter Clement Noel was of African descent and living in America. He had anaemia and chest pains, and in 1910 doctors Ernest Irons and James Herrick looked at his blood under a microscope. What they saw-sickle-shaped red blood cells-was published as the first report of sickle-cell disease.
机译:尼日利亚的伊博族人称他们为奥格邦杰恶意的孩子,注定要懒惰,死亡并反复重生。这些孩子通常困扰着特殊的家庭,这些孩子通常在10岁生日之前死亡。对奥格班杰的信仰已有数百年历史,但距100多年前,人们发现奥格班杰的意义不那么空泛。沃尔特·克莱门特·诺埃尔(Walter Clement Noel)来自非洲,现居美国。他患有贫血和胸痛,在1910年,医生欧内斯特·艾恩斯(Ernest Irons)和詹姆斯·赫里克(James Herrick)在显微镜下观察了他的血液。他们看到镰刀状的红细胞被发表为镰状细胞疾病的首例报道。

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    《The Lancet》 |2013年第9861期|共1页
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