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dc.contributor.authorPEHLIVANOĞLU, Tuna
dc.contributor.authorBALCI, Halil İbrahim
dc.contributor.authorSağlam, Yavuz
dc.contributor.authorDEMIREL, M
dc.contributor.authorDURMAZ, H
dc.date.accessioned2021-03-03T08:36:11Z
dc.date.available2021-03-03T08:36:11Z
dc.identifier.citationPEHLIVANOĞLU T., DEMIREL M., Sağlam Y., BALCI H. İ. , DURMAZ H., "Concomitant rhomboid-shaped tibiae and fibulae, finger-like projections, and orthopedic management in a new variant of nievergelt syndrome: A case report", INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, cilt.42, ss.109-115, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_1871d4d5-3852-48a0-9da8-4bd01b9e9c36
dc.identifier.urihttp://hdl.handle.net/20.500.12627/21739
dc.identifier.urihttps://doi.org/10.1016/j.ijscr.2017.12.002
dc.description.abstractINTRODUCTION: The rare Nievergelt syndrome (NS) is the most severe form of mesomelic dysplasia and is characterized by disproportionate shortness of the limbs. The aim of this case report was to describe the clinical and radiological features of a rare case of NS.
dc.language.isoeng
dc.subjectSurgery
dc.subjectHealth Sciences
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCERRAHİ
dc.titleConcomitant rhomboid-shaped tibiae and fibulae, finger-like projections, and orthopedic management in a new variant of nievergelt syndrome: A case report
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF SURGERY CASE REPORTS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume42
dc.identifier.startpage109
dc.identifier.endpage115
dc.contributor.firstauthorID161444


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