Cited 17 times in

Paleopathological Study of Dwarfism-Related Skeletal Dysplasia in a Late Joseon Dynasty (South Korean) Population

DC Field Value Language
dc.contributor.author우은진-
dc.contributor.author허경석-
dc.contributor.author황재준-
dc.date.accessioned2018-03-26T17:10:24Z-
dc.date.available2018-03-26T17:10:24Z-
dc.date.issued2015-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/157281-
dc.description.abstractSkeletal dysplasias related to genetic etiologies have rarely been reported for past populations. This report presents the skeletal characteristics of an individual with dwarfism-related skeletal dysplasia from South Korea. To assess abnormal deformities, morphological features, metric data, and computed tomography scans are analyzed. Differential diagnoses include achondroplasia or hypochondroplasia, chondrodysplasia, multiple epiphyseal dysplasia, thalassemia-related hemolytic anemia, and lysosomal storage disease. The diffused deformities in the upper-limb bones and several coarsened features of the craniofacial bones indicate the most likely diagnosis to have been a certain type of lysosomal storage disease. The skeletal remains of EP-III-4-No.107 from the Eunpyeong site, although incomplete and fragmented, provide important clues to the paleopathological diagnosis of skeletal dysplasias.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherPublic Library of Science-
dc.relation.isPartOfPLOS ONE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAchondroplasia/diagnosis-
dc.subject.MESHAchondroplasia/genetics-
dc.subject.MESHAdult-
dc.subject.MESHArchaeology/methods*-
dc.subject.MESHBone Diseases, Developmental/diagnosis*-
dc.subject.MESHBone Diseases, Developmental/genetics*-
dc.subject.MESHBone and Bones/abnormalities-
dc.subject.MESHDwarfism/diagnosis-
dc.subject.MESHDwarfism/genetics-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLimb Deformities, Congenital/diagnosis-
dc.subject.MESHLimb Deformities, Congenital/genetics-
dc.subject.MESHLordosis/diagnosis-
dc.subject.MESHLordosis/genetics-
dc.subject.MESHLysosomal Storage Diseases/diagnosis-
dc.subject.MESHLysosomal Storage Diseases/genetics-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMusculoskeletal Abnormalities-
dc.subject.MESHOsteochondrodysplasias/diagnosis-
dc.subject.MESHOsteochondrodysplasias/genetics-
dc.subject.MESHPaleontology/methods*-
dc.subject.MESHPaleopathology/methods*-
dc.subject.MESHRadiometric Dating-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHThalassemia/diagnosis-
dc.subject.MESHThalassemia/genetics-
dc.subject.MESHTomography, X-Ray Computed-
dc.titlePaleopathological Study of Dwarfism-Related Skeletal Dysplasia in a Late Joseon Dynasty (South Korean) Population-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry-
dc.contributor.departmentDept. of Oral Biology-
dc.contributor.googleauthorEun Jin Woo-
dc.contributor.googleauthorWon-Joon Lee-
dc.contributor.googleauthorKyung-Seok Hu-
dc.contributor.googleauthorJae Joon Hwang-
dc.identifier.doi10.1371/journal.pone.0140901-
dc.contributor.localIdA04773-
dc.contributor.localIdA04342-
dc.contributor.localIdA04710-
dc.relation.journalcodeJ02540-
dc.identifier.eissn1932-6203-
dc.identifier.pmid26488291-
dc.contributor.alternativeNameWoo, Eun Jin-
dc.contributor.alternativeNameHu, Kyung Seok-
dc.contributor.alternativeNameHwang, Jae Joon-
dc.contributor.affiliatedAuthorWoo, Eun Jin-
dc.contributor.affiliatedAuthorHu, Kyung Seok-
dc.contributor.affiliatedAuthorHwang, Jae Joon-
dc.citation.volume10-
dc.citation.number10-
dc.citation.startPagee0140901-
dc.identifier.bibliographicCitationPLOS ONE, Vol.10(10) : e0140901, 2015-
dc.identifier.rimsid42319-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Oral and Maxillofacial Radiology (영상치의학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.