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dc.contributor.author박은애-
dc.contributor.author김경효-
dc.date.accessioned2017-08-29T03:34:14Z-
dc.date.available2017-08-29T03:34:14Z-
dc.date.issued2013-
dc.identifier.issn1783-1061-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/229893-
dc.description.abstractSternal malformation/vascular dysplasia association is a rare congenital dysmorphology, which has not yet been reported in Korea. Its typical clinical features include a sternal cleft covered with atrophic skin, a median abdominal raphe extending from the sternal defect to the umbilicus, and cutaneous craniofacial hemangiomata. We report a case of a full-term newborn who presented with no anomalies at birth, except for a skin defect over the sternum and a supraumbilical raphe. Multiple hemangiomas appeared subsequently on her chin and upper chest wall, and respiratory distress due to subglottic hemangioma developed during the first 2 months of life. Her symptoms were controlled with oral prednisolone administration. No respiratory distress have recurred during the 3-year follow-up period. © 2013 by The Korean Pediatric Society.-
dc.languageEnglish-
dc.titleA girl with sternal malformation/vascular dysplasia association-
dc.typeArticle-
dc.relation.issue3-
dc.relation.volume56-
dc.relation.indexSCOPUS-
dc.relation.startpage135-
dc.relation.lastpage138-
dc.relation.journaltitleKorean Journal of Pediatrics-
dc.identifier.doi10.3345/kjp.2013.56.3.135-
dc.identifier.scopusid2-s2.0-84875163012-
dc.author.googleLee N.Y.-
dc.author.googleCho H.K.-
dc.author.googleKim K.-H.-
dc.author.googlePark E.A.-
dc.contributor.scopusid박은애(14424551500)-
dc.contributor.scopusid김경효(35448653000)-
dc.date.modifydate20180104081001-
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의학전문대학원 > 의학과 > Journal papers
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