When to suspect primary ciliary dyskinesia in children

被引：10
作者：
Fitzgerald, Dominic A. [1 ,2 ]
Shapiro, Adam J. [3 ]
机构：
[1] Childrens Hosp Westmead, Dept Resp Med, Sydney, NSW, Australia
[2] Univ Sydney, Sydney Med Sch, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
[3] McGill Univ, Montreal Childrens Hosp, Pediat Resp Med, 1001 Decarie Blvd BRC-5016, Montreal, PQ H4A 3J1, Canada
来源：
PAEDIATRIC RESPIRATORY REVIEWS | 2016年 / 18卷
关键词：
Primary Ciliary Dyskinesia [PCD; neonatal respiratory distress; situs inversus; persistent rhinosinusitis; chronic wet cough; CONGENITAL HEART-DISEASE; CHRONIC WET COUGH; POLYCYSTIC KIDNEY-DISEASE; RESPIRATORY-DISTRESS; KARTAGENER-SYNDROME; CLINICAL-FEATURES; NITRIC-OXIDE; HETEROTAXY; DIAGNOSIS; BRONCHIECTASIS;
D O I：
10.1016/j.prrv.2015.11.006
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Primary ciliary dyskinesia [PCD] is an uncommon, autosomal recessively inherited condition that is often overlooked and undertreated in childhood. Amidst the myriad of children with coloured nasal secretions, otitis media and a wet cough, there exists a subset with PCD as the underlying unifying diagnosis. In this paper we have highlighted the varying clinical manifestations of PCD, emphasising different presentations between neonates, toddlers, school aged children and adults. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码：3 / 7
页数：5
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