Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 박은애 | * |
dc.contributor.author | 김경효 | * |
dc.date.accessioned | 2016-08-28T11:08:06Z | - |
dc.date.available | 2016-08-28T11:08:06Z | - |
dc.date.issued | 2013 | * |
dc.identifier.issn | 1783-1061 | * |
dc.identifier.other | OAK-13954 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/229893 | - |
dc.description.abstract | Sternal 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.language | English | * |
dc.title | A girl with sternal malformation/vascular dysplasia association | * |
dc.type | Article | * |
dc.relation.issue | 3 | * |
dc.relation.volume | 56 | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 135 | * |
dc.relation.lastpage | 138 | * |
dc.relation.journaltitle | Korean Journal of Pediatrics | * |
dc.identifier.doi | 10.3345/kjp.2013.56.3.135 | * |
dc.identifier.scopusid | 2-s2.0-84875163012 | * |
dc.author.google | Lee N.Y. | * |
dc.author.google | Cho H.K. | * |
dc.author.google | Kim K.-H. | * |
dc.author.google | Park E.A. | * |
dc.contributor.scopusid | 박은애(14424551500) | * |
dc.contributor.scopusid | 김경효(35448653000) | * |
dc.date.modifydate | 20240301081003 | * |