dc.creatorAggarwal, Varun
dc.creatorImamura, Michaki
dc.creatorAcuña Aguirre, Carlos
dc.creatorCabrera, Antonio G.
dc.date.accessioned2018-07-23T16:59:50Z
dc.date.available2018-07-23T16:59:50Z
dc.date.created2018-07-23T16:59:50Z
dc.date.issued2018
dc.identifierCardiology in The Young, 28 (3): 467-470
dc.identifier10.1017/S104795111700227X
dc.identifierhttps://repositorio.uchile.cl/handle/2250/150157
dc.description.abstractIn this study, we report a patient with pulmonary atresia with intact ventricular septum (PA/IVS), confluent pulmonary arteries supplied by an arterial duct, and chromosome 22q11.2 microdeletion. The 22q11.2 deletion syndrome has been associated with anomalies of the outflow tracts, such as tetralogy of Fallot with either pulmonary stenosis or atresia, but we are aware of a solitary case described with pulmonary atresia when the ventricular septum is intact. The presence of genetic malformations can have long-term co-morbidities. By describing our patient, we aim to create awareness of this rare association.
dc.languageen
dc.publisherCambridge University Press
dc.sourceCardiology in The Young
dc.subjectChromosome 22q11 deletion
dc.subjectPulmonary atresia
dc.subjectIntact ventricular septum
dc.subjectConfluent branch pulmonary arteries
dc.subjectRight aortic arch
dc.titleChromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries
dc.typeArtículo de revista


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