遗传性球形红细胞增多症
Hereditary spherocytosis.
作者信息
Huq Sayeeda, Pietroni Mark A C, Rahman Hafizur, Alam Mohammad Tariqul
机构信息
Clinical Sciences Division, ICDDR,B, GPO Box 128, Dhaka 1000, Bangladesh.
出版信息
J Health Popul Nutr. 2010 Feb;28(1):107-9. doi: 10.3329/jhpn.v28i1.4529.
A 12-year-old girl was brought to the Dhaka Hospital of ICDDR,B with diarrhoea. Incidentally, the parents provided a history of repeated episodes of pallor and jaundice since she was two and half years old. Three of her family members had similar problems. History, clinical examination, and laboratory findings of the girl and her family members suggested a case of hereditary spherocytosis. To our knowledge, this is the first report of such a case in Bangladesh.
一名12岁女孩因腹泻被送往达卡国际腹泻病研究中心孟加拉国医院。偶然间，其父母提供了自她两岁半起就反复出现面色苍白和黄疸的病史。她的三名家庭成员也有类似问题。该女孩及其家庭成员的病史、临床检查和实验室检查结果提示为遗传性球形红细胞增多症。据我们所知，这是孟加拉国首例此类病例报告。
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