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阿拉伯儿童先天性再生障碍性贫血(戴蒙德-布莱克范综合征)。

Congenital hypoplastic anaemia in Arab children (Diamond-Blackfan syndrome).

作者信息

Lubani M M, Sharda D C, Qattawi S A, Al-Shab T, Hassanein A A

机构信息

Department of Paediatrics, Farwaniya Hospital, Kuwait.

出版信息

Ann Trop Paediatr. 1987 Sep;7(3):227-31. doi: 10.1080/02724936.1987.11748513.

DOI:10.1080/02724936.1987.11748513
PMID:2445276
Abstract

Three Arab children with congenital hypoplastic anaemia are reported. The three children presented with pallor in the first 3 months of life. All were given corticosteroids at different times. The first child is on high doses of prednisone and also needs blood transfusion every 6 weeks. The second child is on 5 mg prednisone every other day and is in remission. The third has been in complete remission for the last 5 years and is on no treatment. None of these children has associated congenital or chromosomal abnormalities.

摘要

报告了三名患有先天性再生障碍性贫血的阿拉伯儿童。这三名儿童在出生后的前3个月出现面色苍白。所有患儿均在不同时间接受了皮质类固醇治疗。第一名儿童正在服用高剂量泼尼松,并且每6周需要输血一次。第二名儿童每隔一天服用5毫克泼尼松,目前处于缓解期。第三名儿童在过去5年中一直处于完全缓解状态,未接受任何治疗。这些儿童均无相关的先天性或染色体异常。

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Ann Trop Paediatr. 1987 Sep;7(3):227-31. doi: 10.1080/02724936.1987.11748513.
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