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一名因多种活动纤毛生成减少继发支气管扩张的患者中发现新型细胞周期蛋白O致病变体。

Novel CYCLIN-O pathogenic variants in a patient presenting with bronchiectasis secondary to reduced generation of multiple motile cilia.

作者信息

Yap Kim Hoong, Lim Albert Yick Hou, Thomas Biju, Bonnard Carine, Szenker-Ravi Emmanuelle, Chong Yan Ling, Roy Sudipto, Reversade Bruno

机构信息

Department of Respiratory & Critical Care Medicine Tan Tock Seng Hospital Singapore.

Lee Kong Chian School of Medicine Nanyang Technological University Singapore.

出版信息

Respirol Case Rep. 2024 Oct 29;12(11):e70057. doi: 10.1002/rcr2.70057. eCollection 2024 Nov.

DOI:10.1002/rcr2.70057
PMID:39479223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11519382/
Abstract

Reduced generation of multiple motile cilia (RGMC) represents a rare variant of Primary Ciliary Dyskinesia (PCD), associated with mutations. We report a novel compound mutation in the gene in an adult Chinese Singaporean exhibiting chronic productive cough since childhood and recurrent sino-pulmonary infections. Low nasal nitric oxide and bronchiectasis suggests PCD. Bronchoscopy for epithelial and nasal brushings for ciliary studies were repeated after adequate treatment of lower respiratory tract infections. Demonstration of oligo-cilia via transmission electron microscopy, and detection of mutation through genetic analysis were utilized to diagnose RGMC. Repeated courses of antibiotics including nebulised antibiotics were used to treat recurrent infections and exacerbations. Airway clearance techniques, immunizations and collaboration with otorhinolaryngologist form part of the long-term management. Heightened clinical suspicion and adherence to established diagnostic algorithms are essential for timely recognition of this entity.

摘要

多发性活动纤毛生成减少(RGMC)是原发性纤毛运动障碍(PCD)的一种罕见变异型,与基因突变有关。我们报告了一名成年华裔新加坡人该基因中的一种新型复合突变,该患者自童年起就患有慢性咳痰性咳嗽和反复的鼻窦肺部感染。低鼻一氧化氮水平和支气管扩张提示为PCD。在下呼吸道感染得到充分治疗后,重复进行支气管镜检查以获取上皮细胞样本,并进行鼻刷检以进行纤毛研究。通过透射电子显微镜证实存在少纤毛,并通过基因分析检测到突变,以此诊断RGMC。使用包括雾化抗生素在内的反复抗生素疗程来治疗反复感染和病情加重。气道清除技术、免疫接种以及与耳鼻喉科医生的协作是长期管理的一部分。提高临床怀疑度并遵循既定的诊断算法对于及时识别该疾病至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c52/11519382/a4fa467cf44b/RCR2-12-e70057-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c52/11519382/2f46b6ae5e1b/RCR2-12-e70057-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c52/11519382/a4fa467cf44b/RCR2-12-e70057-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c52/11519382/2f46b6ae5e1b/RCR2-12-e70057-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c52/11519382/a4fa467cf44b/RCR2-12-e70057-g001.jpg

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1
Novel CYCLIN-O pathogenic variants in a patient presenting with bronchiectasis secondary to reduced generation of multiple motile cilia.一名因多种活动纤毛生成减少继发支气管扩张的患者中发现新型细胞周期蛋白O致病变体。
Respirol Case Rep. 2024 Oct 29;12(11):e70057. doi: 10.1002/rcr2.70057. eCollection 2024 Nov.
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本文引用的文献

1
European Respiratory Society guidelines for the management of adult bronchiectasis.欧洲呼吸学会成人支气管扩张症管理指南。
Eur Respir J. 2017 Sep 9;50(3). doi: 10.1183/13993003.00629-2017. Print 2017 Sep.
2
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.特定人群中CCNO变异体的系统分析:对临床表型和鉴别诊断的意义
Hum Mutat. 2016 Apr;37(4):396-405. doi: 10.1002/humu.22957. Epub 2016 Feb 4.
3
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.
CCNO 基因突变导致先天性黏液纤毛清除障碍,导致多种运动纤毛生成减少。
Nat Genet. 2014 Jun;46(6):646-51. doi: 10.1038/ng.2961. Epub 2014 Apr 20.
4
A method and server for predicting damaging missense mutations.一种预测有害错义突变的方法及服务器。
Nat Methods. 2010 Apr;7(4):248-9. doi: 10.1038/nmeth0410-248.