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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Ulster Medical Society
2009
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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. |
format | Text |
id | pubmed-2629012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Ulster Medical Society |
record_format | MEDLINE/PubMed |
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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