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DNA连接酶4缺乏症致反复肺炎1例报告

One case report on recurrent pneumonia due to DNA ligase Ⅳ deficiency
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摘要 DNA连接酶4缺乏症(DNA ligase IV syndrome,LIG4),又称LIG4综合征(OMIO#606593),是一种与联合免疫缺陷相关的罕见常染色体隐性遗传病。临床主要表现为小头畸形、鸟样面容、生长发育迟缓、皮肤异常和全血细胞减少[1]。本文报告1例LIG4综合征患儿的临床资料,并回顾国内外相关病例的临床特征,以提高临床医师对该疾病的认识。1病历资料患儿女,2岁1月龄,因咳嗽伴喘息半个月入院。咳嗽无明显诱因,伴喘息,起病6 d后咳嗽渐加重,偶可呕出大量黄色及白色黏痰。
作者 薛仁杰 田曼 赵德育 包玉玲 顾海燕 王娅萍 王筠 XUE Ren-jie;TIAN Man;ZHAO De-yu
出处 《中国实用儿科杂志》 CSCD 北大核心 2020年第6期490-492,共3页 Chinese Journal of Practical Pediatrics
关键词 DNA连接酶4缺乏症 严重联合免疫缺陷病 反复肺炎 小头畸形 鸟样面容 DNA ligaseⅣdeficiency severe combined immunodeficiency disease recurrent pneumonia microcephaly bird-like face
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