Hereditary spherocytosis in a Negro family; report of three cases.

W. Esmond, C. L. Quinn, H. Peters
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引用次数: 1

Abstract

There are only 14 case reports of hereditary spherocytosis among American Negroes. We have recently had the opportunity of studying three Negro children with this disorder from the same family. REPORT OF CASES Case1.—On March 5, 1955, a 14-year-old Negro youth was seen for the first time in the accident room of Mercy Hospital. The patient was seen lying on the examining cot in an attitude of flexion on his left side and appeared acutely ill. His respirations were rapid and shallow, and he was unable to give an account of his present illness. The patient's mother and father supplied the necessary information, and stated that nine days previously the patient, who had been in good health, suddenly developed chills and fever. The patient's family physician was called. He examined the patient, stated that he had a viral infection, and prescribed an unknown medication. The patient was seen two
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黑人家族遗传性球形红细胞增多症的研究报告三例病例。
在美国黑人中只有14例遗传性球形红细胞增多症的报告。我们最近有机会研究来自同一家庭的三个患有这种疾病的黑人儿童。病例报告1。1955年3月5日,一个14岁的黑人青年第一次出现在仁爱医院的急诊室。病人被看到躺在检查床上,在他的左屈的态度,并出现急性疾病。他的呼吸急促而微弱,他说不出他目前的病情。病人的母亲和父亲提供了必要的资料,并说,9天前,一直健康的病人突然发冷和发烧。病人的家庭医生被叫来了。他给病人做了检查,说他感染了病毒,并开了一种不知名的药。病人看了两遍
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