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The patient’s experience of primary ciliary dyskinesia: a systematic review

BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary disease, with symptoms starting soon after birth. The aim of this study is to critically review, analyse, and synthesise the literature in order to understand the experiences of patient...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Qual Life Res
Main Authors: Behan, Laura, Rubbo, Bruna, Lucas, Jane S., Dunn Galvin, Audrey
Format: Artigo
Jezik:Inglês
Izdano: Springer International Publishing 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5548843/
https://ncbi.nlm.nih.gov/pubmed/28361274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11136-017-1564-y
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