Show simple item record

dc.contributor.authorSmith, A.
dc.contributor.authorRyan, E
dc.contributor.authorO’Keeffe, D
dc.contributor.authorO’Donovan, D.
dc.date.accessioned2019-04-02T09:05:45Z
dc.date.available2019-04-02T09:05:45Z
dc.date.issued2019-03
dc.identifier.urihttp://hdl.handle.net/10147/624154
dc.description.abstractCystic Fibrosis (CF) is the most common genetically inherited disease in Ireland1. Approximately 1/ 2,300 infants per year are born with CF in Ireland2. Newborn bloodspot screening (NBS) screening for CF was introduced to Ireland in 20113. NBS screening for CF is associated with improved lung function, nutritional status and increased survival into early adulthood4. Therefore early recognition and management of this chronic condition is vital to ensuring optimal patient management.en_US
dc.language.isoenen_US
dc.publisherIrish Medical Journalen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectCYSTIC FIBROSISen_US
dc.subjectNEWBORN SCREENINGen_US
dc.titleMeconium Ileus in Two Irish Newborns: The Presenting Feature of Cystic Fibrosisen_US
dc.typeArticleen_US
dc.identifier.journalIrish Medical Journalen_US
dc.description.fundingNo fundingen_US
dc.description.provinceConnachten_US
dc.description.peer-reviewpeer-reviewen_US
refterms.dateFOA2019-04-02T09:05:45Z


Files in this item

Thumbnail
Name:
art9.html
Size:
34.61Kb
Format:
HTML
Description:
Main Article

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States