摘要
先天性角化不良(dyskeratosis Congenita,DC)是临床上一种少见的以皮肤异常色素沉着、指(趾)甲营养不良及黏膜白斑为特征的遗传性疾病[1],同时合并肺间质纤维化的更为罕见,国外文献报道DC中约有20%合并肺间质纤维化[2],国内目前尚无报道,现将郑州大学第一附属医院收治的1例DC合并肺间质纤维化患者诊治经验报道如下.
出处
《中华结核和呼吸杂志》
CAS
CSCD
北大核心
2015年第9期701-703,共3页
Chinese Journal of Tuberculosis and Respiratory Diseases
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共引文献14
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4李芬宇,郭红霞,罗琴,杨晓红,赵蕾,吐尔逊古丽.特发性肺间质纤维化急性加重的6例报导并文献复习[J].新疆医学,2009,38(7):34-37. 被引量:2
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5张德平.过敏性肺炎的诊断[J].临床肺科杂志,2011,16(7):985-986. 被引量:8
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同被引文献7
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4赵惠君,谢晓恬.Wiskott-Aldrich综合征患儿临床特征与诊断治疗[J].中华实用儿科临床杂志,2015,30(9):685-688. 被引量:9
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5万扬,安文彬,张家源,章婧嫽,张然然,朱帅,常丽贤,张英驰,刘芳,杨文钰,陈晓娟,邹尧,陈玉梅,竺晓凡.八例先天性角化不良伴骨髓衰竭患儿的临床特征及基因分析[J].中华血液学杂志,2016,37(3):216-220. 被引量:2
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6黄珍,陈敏,李原,徐智胜,钱江潮,周海霞,王菊香.一例先天性角化不良患儿的基因变异研究[J].中华医学遗传学杂志,2020,37(1):86-88. 被引量:1
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7黄茂欣,于建斌,刘莉娜,李小红,张江安.常染色体隐性遗传先天性角化不良一例及TERT基因突变研究[J].中华皮肤科杂志,2020,53(11):875-879. 被引量:1
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