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一名具有希腊血统的美国白人男孩患镰状细胞贫血。

Sickle cell anemia in an American white boy of Greek ancestry.

作者信息

Campbell J J, Oski F A

出版信息

Am J Dis Child. 1977 Feb;131(2):186-8. doi: 10.1001/archpedi.1977.02120150068013.

Abstract

A 7-year-old American white boy of Greek ancestry had sickle cell anemia. The disease in this patient was not accompanied by painful episodes or recognizable hematologic complications, although he did demonstrate considerable delay in skeletal maturation. The patient sought medical attention for a dermatologic problem that was ultimately diagnosed as pityriasis rubra pilaris. To our knowledge, this is the first demonstrated example of sickle cell anemia in a white male described in the United States.

摘要

一名7岁有希腊血统的美国白人男孩患有镰状细胞贫血。该患者的疾病未伴有疼痛发作或可识别的血液学并发症,尽管他确实表现出骨骼成熟明显延迟。该患者因皮肤问题就医,最终被诊断为毛发红糠疹。据我们所知,这是美国描述的首例白人男性镰状细胞贫血病例。

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