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A Novel Noonan Syndrome RAF1 Mutation: Lethal Course in a Preterm Infant

dc.contributor.authorRatola, A.
dc.contributor.authorSilva, H.
dc.contributor.authorGuedes, A.
dc.contributor.authorMota, C.
dc.contributor.authorBraga, A.
dc.contributor.authorOliveira, D.
dc.contributor.authorAlegria, A.
dc.contributor.authorCarvalho, C.
dc.contributor.authorÁlvares, S.
dc.contributor.authorProença, E.
dc.date.accessioned2016-07-26T13:50:11Z
dc.date.available2016-07-26T13:50:11Z
dc.date.issued2015
dc.description.abstractNoonan syndrome is a relatively common and heterogeneous genetic disorder, associated with congenital heart defect in about 50% of the cases. If the defect is not severe, life expectancy is normal. We report a case of Noonan syndrome in a preterm infant with hypertrophic cardiomyopathy and lethal outcome associated to acute respiratory distress syndrome caused by Adenovirus pneumonia. A novel mutation in the RAF1 gene was identified: c.782C>G (p.Pro261Arg) in heterozygosity, not described previously in the literature. Consequently, the common clinical course in this mutation and its respective contribution to the early fatal outcome is unknown. No conclusion can be established regarding genotype/phenotype correlation.pt_PT
dc.identifier.citationPediatr Rep. 2015;7(2):5955pt_PT
dc.identifier.doi10.4081/pr.2015.5955pt_PT
dc.identifier.issn2036-7503
dc.identifier.urihttp://hdl.handle.net/10400.16/1978
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherPAGEpresspt_PT
dc.relation.publisherversionhttp://www.pagepress.org/journals/index.php/pr/article/view/5955/4692pt_PT
dc.titleA Novel Noonan Syndrome RAF1 Mutation: Lethal Course in a Preterm Infantpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceItalypt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage5955pt_PT
oaire.citation.titlePediatric Reportspt_PT
oaire.citation.volume7pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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