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dc.contributor.authorSaviga Sethasathienen_US
dc.contributor.authorMallika Pomropen_US
dc.contributor.authorKwannapas Saengsinen_US
dc.contributor.authorVarangthip Khuwuthyakornen_US
dc.contributor.authorSuchaya Silvilairaten_US
dc.date.accessioned2020-04-02T15:12:24Z-
dc.date.available2020-04-02T15:12:24Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn2347193Xen_US
dc.identifier.issn22114122en_US
dc.identifier.other2-s2.0-85078906209en_US
dc.identifier.other10.4103/jcecho.jcecho_30_19en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85078906209&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/67957-
dc.description.abstract© 2020 Journal of Cardiovascular Echography | Published by Wolters Kluwer ? Medknow. The draining of the right superior vena cava (SVC) into the left atrium is a very rare anomaly of systemic vein drainage. This case report describes a term male infant presenting with central cyanosis diagnosed with right SVC drainage into the left atrium. The diagnosis was performed using conventional echocardiography and computed tomography angiography. Surgical correction with translocation of the right SVC to the right atrium was necessary to treat the symptom of cyanosis and prevent further complications, including brain abscesses and paradoxical embolization.en_US
dc.subjectMedicineen_US
dc.titleNeonatal central cyanosis caused by anomalous drainage of the right superior vena cavaen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Cardiovascular Echographyen_US
article.volume29en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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