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Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)

Surfactant deficiency and the resultant respiratory distress syndrome (RDS) seen in preterm infants is a major cause of respiratory morbidity in this population. Until recently, the contribution of surfactant to respiratory morbidity in infancy was limited to the neonatal period. It is now recognise...

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Detalles Bibliográficos
Autores principales: McFetridge, Lynne, McMorrow, Aoife, Morrison, Patrick J, Shields, Michael D
Formato: Texto
Lenguaje:English
Publicado: The Ulster Medical Society 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629012/
https://www.ncbi.nlm.nih.gov/pubmed/19252722
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author McFetridge, Lynne
McMorrow, Aoife
Morrison, Patrick J
Shields, Michael D
author_facet McFetridge, Lynne
McMorrow, Aoife
Morrison, Patrick J
Shields, Michael D
author_sort McFetridge, Lynne
collection PubMed
description Surfactant deficiency and the resultant respiratory distress syndrome (RDS) seen in preterm infants is a major cause of respiratory morbidity in this population. Until recently, the contribution of surfactant to respiratory morbidity in infancy was limited to the neonatal period. It is now recognised that inborn errors of surfactant metabolism leading to surfactant dysfunction account for around 10% of childhood interstitial lung disease (chILD). These abnormalities can be detected by blood sampling for mutation analysis, thereby avoiding the need for lung biopsy in some children with chILD.
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spelling pubmed-26290122009-03-01 Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD) McFetridge, Lynne McMorrow, Aoife Morrison, Patrick J Shields, Michael D Ulster Med J Review Surfactant deficiency and the resultant respiratory distress syndrome (RDS) seen in preterm infants is a major cause of respiratory morbidity in this population. Until recently, the contribution of surfactant to respiratory morbidity in infancy was limited to the neonatal period. It is now recognised that inborn errors of surfactant metabolism leading to surfactant dysfunction account for around 10% of childhood interstitial lung disease (chILD). These abnormalities can be detected by blood sampling for mutation analysis, thereby avoiding the need for lung biopsy in some children with chILD. The Ulster Medical Society 2009-01 /pmc/articles/PMC2629012/ /pubmed/19252722 Text en © The Ulster Medical Society, 2009
spellingShingle Review
McFetridge, Lynne
McMorrow, Aoife
Morrison, Patrick J
Shields, Michael D
Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title_full Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title_fullStr Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title_full_unstemmed Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title_short Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
title_sort surfactant metabolism dysfunction and childhood interstitial lung disease (child)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629012/
https://www.ncbi.nlm.nih.gov/pubmed/19252722
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