The impact of Primary Ciliary Dyskinesia on the upper respiratory tract.

Abstract:

:Primary Ciliary Dyskinesia (PCD) is an autosomal recessive genetic condition affecting the function of motile cilia. The upper respiratory tract is lined with ciliated epithelium and hence a hallmark of PCD is the development, from the neonatal period onwards, of persisting secretion retention and suppurative infection in the middle ear, nose and facial sinuses [1]. This review aims to remind the clinician involved in the care of a patient with PCD of the complexities of making the diagnosis of chronic rhinosinusitis (CRS) and chronic otitis media with effusion (ChOME), the morbidity associated with CRS and ChOME and of current evidence of best practice for the management of these conditions.

journal_name

Paediatr Respir Rev

authors

Morgan LC,Birman CS

doi

10.1016/j.prrv.2015.09.006

subject

Has Abstract

pub_date

2016-03-01 00:00:00

pages

33-8

eissn

1526-0542

issn

1526-0550

pii

S1526-0542(15)00091-3

journal_volume

18

pub_type

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