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鼻窦炎-中耳炎-双肺弥漫支气管扩张
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作者 周王继 赵新月 +3 位作者 刘雅萍 郑姝颖 徐凯峰 田欣伦 《中华结核和呼吸杂志》 CAS CSCD 北大核心 2022年第11期1117-1120,共4页
原发性纤毛运动障碍(PCD)是一种罕见的常染色体隐性或X连锁相关的双等位基因变异遗传病,以纤毛运动障碍为特征。典型表现包括支气管扩张、分泌性中耳炎、鼻窦炎、内脏反位和不孕不育等,常因临床表现相似需与囊性纤维化(CF)鉴别。本文介... 原发性纤毛运动障碍(PCD)是一种罕见的常染色体隐性或X连锁相关的双等位基因变异遗传病,以纤毛运动障碍为特征。典型表现包括支气管扩张、分泌性中耳炎、鼻窦炎、内脏反位和不孕不育等,常因临床表现相似需与囊性纤维化(CF)鉴别。本文介绍1例幼年起反复咳嗽、咳痰伴发热的青少年女性,有分泌性中耳炎、鼻窦炎病史,曾考虑诊断CF。后经基因测序发现PCD相关致病基因复合杂合变异,结合临床表现、影像学特点,最终诊断为PCD。 展开更多
关键词 支气管扩张 鼻窦炎 青少年女性 常染色体隐性 囊性纤维化 不孕不育 分泌性中耳炎 内脏反位
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Case report of neurofibromatosis type 1 combined with primary ciliary dyskinesia 被引量:2
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作者 Chun Bian Xinyue Zhao +4 位作者 Yaping Liu Minjiang Chen shuying zheng Xinlun Tian Kai-Feng Xu 《Frontiers of Medicine》 SCIE CSCD 2021年第6期933-937,共5页
Neurofibromatosis(NF)is a genetic disease in which the lungs are rarely involved.However,in NF cases with lung involvement,chest computed tomography may show bilateral basal reticulations,apical bullae,and cysts witho... Neurofibromatosis(NF)is a genetic disease in which the lungs are rarely involved.However,in NF cases with lung involvement,chest computed tomography may show bilateral basal reticulations,apical bullae,and cysts without bronchiectasis.Herein,we report a patient diagnosed with NF on the basis of the results of genetic testing who presented with early-onset wet cough and bronchiectasis.Considering the differential diagnosis of bronchiectasis combined with his early-onset wet cough,sinusitis,and sperm quality decline,we considered the possibility of primary ciliary dyskinesia(PCD).Further electron microscopy analysis of cilia and identification of homozygous mutations in the RSPH4A gene confirmed the diagnosis of PCD.Therefore,for patients with NF,when an image change exists in the lungs that does not correspond to NF,the possibility of other diagnoses,including PCD,must be considered. 展开更多
关键词 primary ciliary dyskinesia NEUROFIBROMATOSIS BRONCHIECTASIS transmission electron microscopy genetic sequencing
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