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XYY syndrome: a 13-year-old boy with tall stature

DC Field Value Language
dc.contributor.author권아름-
dc.contributor.author김호성-
dc.contributor.author정모경-
dc.contributor.author조원하-
dc.contributor.author채현욱-
dc.date.accessioned2018-03-26T16:41:03Z-
dc.date.available2018-03-26T16:41:03Z-
dc.date.issued2015-
dc.identifier.issn2287-1012-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/156708-
dc.description.abstractWhen evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess growth hormone secretion, Marfan syndrome, androgen or estrogen deficiency, testicular feminization, and sex chromosome anomaly, such as Klinefelter syndrome and XYY syndrome. Men with 47,XYY syndrome can exhibit multiple phenotypes. A 13-year-old boy visited the hospital for evaluation of tall stature. The boy had no other physical abnormalities except tall stature. All biochemical and imaging studies were within the normal ranges. He was diagnosed with XYY syndrome in this chromosome study. When evaluating men with tall stature, XYY syndrome should be ruled out.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherKorean Society of Pediatric Endocrinology-
dc.relation.isPartOfANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleXYY syndrome: a 13-year-old boy with tall stature-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Pediatrics-
dc.contributor.googleauthorWon Ha Jo-
dc.contributor.googleauthorMo Kyung Jung-
dc.contributor.googleauthorKi Eun Kim-
dc.contributor.googleauthorHyun Wook Chae-
dc.contributor.googleauthorDuk Hee Kim-
dc.contributor.googleauthorAh Reum Kwon-
dc.contributor.googleauthorHo-Seong Kim-
dc.identifier.doi10.6065/apem.2015.20.3.170-
dc.contributor.localIdA00228-
dc.contributor.localIdA01184-
dc.contributor.localIdA03599-
dc.contributor.localIdA04681-
dc.contributor.localIdA04026-
dc.relation.journalcodeJ00175-
dc.identifier.eissn2287-1292-
dc.identifier.pmid26512355-
dc.subject.keyword47,XYY syndrome-
dc.subject.keywordGrowth disorders-
dc.subject.keywordSex chromosome disorders-
dc.contributor.alternativeNameKwon, Ah Reum-
dc.contributor.alternativeNameKim, Ho Seong-
dc.contributor.alternativeNameJung, Mo Kyung-
dc.contributor.alternativeNameJo, Won Ha-
dc.contributor.alternativeNameChae, Hyun Wook-
dc.contributor.affiliatedAuthorKwon, Ah Reum-
dc.contributor.affiliatedAuthorKim, Ho Seong-
dc.contributor.affiliatedAuthorJung, Mo Kyung-
dc.contributor.affiliatedAuthorJo, Won Ha-
dc.contributor.affiliatedAuthorChae, Hyun Wook-
dc.citation.volume20-
dc.citation.number3-
dc.citation.startPage170-
dc.citation.endPage173-
dc.identifier.bibliographicCitationANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, Vol.20(3) : 170-173, 2015-
dc.identifier.rimsid39838-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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