Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/4129
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dc.contributor.authorSreeram, Narayanswami
dc.contributor.authorPretel, E.
dc.contributor.authorPillekamp, Frank
dc.contributor.authorBennink, Gerardus
dc.date.accessioned2015-07-16T05:48:02Z
dc.date.available2015-07-16T05:48:02Z
dc.date.issued2008
dc.identifier.citationImages in Paediatric Cardiology. 2008, Vol.10(4), p. 1-4en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/4129
dc.description.abstractScimitar syndrome, if presenting in infancy, is associated with signs of heart failure and pulmonary hypertension. The typical pathological features are sequestration of a segment of the lung, usually the right lower lobe, with arterial supply arising from the abdominal aorta, and partial anomalous pulmonary venous connection, with the sequestered segment draining to the inferior caval vein. The typical angiographic features of an infant with Scimitar syndrome. is presented in this articleen_GB
dc.language.isoenen_GB
dc.publisherImages in Paediatric Cardiologyen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectCardiac catheterizationen_GB
dc.subjectScimitar syndromeen_GB
dc.subjectCongenital heart diseaseen_GB
dc.subjectPediatricsen_GB
dc.titleScimitar syndrome in infancyen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
Appears in Collections:IPC, Volume 10, Issue 4
IPC, Volume 10, Issue 4

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