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Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
Authors:Lynne McFetridge   Aoife McMorrow   Patrick J Morrison     Michael D Shields
Affiliation:1.Royal Belfast Hospital for Sick Children, Grosvenor Road, Belfast BT12 6BA. United Kingdom;2.Department of Child Health, Queens University Belfast, Grosvenor Road, Belfast BT12 6BA. United Kingdom;3.Northern Ireland Regional Genetics Centre, Belfast Trust, Belfast BT9 7AB, United Kingdom
Abstract: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.
Keywords:Surfactant   child   mutation analysis
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