Accessory liver in an infant with congenital diaphragmatic hernia.

dc.contributor.author	Beiler, Hans Albert	en
dc.contributor.author	Sergi, C.	en
dc.contributor.author	Wagner, G.	en
dc.contributor.author	Zachariou, Zacharias	en
dc.creator	Beiler, Hans Albert	en
dc.creator	Sergi, C.	en
dc.creator	Wagner, G.	en
dc.creator	Zachariou, Zacharias	en
dc.date.accessioned	2018-06-22T09:52:31Z
dc.date.available	2018-06-22T09:52:31Z
dc.date.issued	2001
dc.identifier.uri	https://gnosis.library.ucy.ac.cy/handle/7/41400
dc.description.abstract	Incidence of congenital diaphragmatic hernia (CDH) ranges from 1 in 2,400 to one in 5,000 live births. Associated anomalies in CDH are approximately 30% to 35%. The authors report on an infant with CDH and an accessory supradiaphragmatic liver with separate vascularization from the thoracic aorta. The pathogenesis of this malformation is discussed. The postoperative course and the follow-up of the child over 5 years was completely uneventful. Copyright 2001 by W.B. Saunders Company.	en
dc.language.iso	eng	en
dc.source	Journal of pediatric surgery	en
dc.title	Accessory liver in an infant with congenital diaphragmatic hernia.	en
dc.type	info:eu-repo/semantics/article
dc.description.volume	36
dc.description.issue	6
dc.author.faculty	Ιατρική Σχολή / Medical School
dc.author.department	Ιατρική Σχολή / Medical School
dc.type.uhtype	Article	en
dc.contributor.orcid	Zachariou, Zacharias [0000-0001-8305-8037]
dc.gnosis.orcid	0000-0001-8305-8037

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