Publication:
An uncommon reason of osteoporosis: Spondyloepiphyseal dysplasia congenita

dc.contributor.authorElbasan, Onur
dc.contributor.authorŞişman, Pınar
dc.contributor.authorGül, Özen Öz
dc.contributor.authorCander, Soner
dc.contributor.authorErsoy, Canan
dc.contributor.buuauthorElbasan, Onur
dc.contributor.buuauthorÖZ GÜL, ÖZEN
dc.contributor.buuauthorCANDER, SONER
dc.contributor.buuauthorERSOY, CANAN
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.departmentEndokrinoloji ve Metabolizma Hastalıkları Bilim Dalı
dc.contributor.researcheridAAI-1005-2021
dc.contributor.researcheridABF-5216-2021
dc.contributor.researcheridAAH-8861-2021
dc.contributor.researcheridCJH-1319-2022
dc.date.accessioned2024-10-15T11:11:24Z
dc.date.available2024-10-15T11:11:24Z
dc.date.issued2017-12-01
dc.description.abstractSkeletal dysplasia is a complex and rare disease group that presents with clinical and radiological findings that differ from classical metabolic bone diseases in which bone and cartilage tissue are affected together. Spondyloepiphyseal dysplasia conjenita with involvement of the spine and long bone epiphyses is seen with short stature and short body from birth. Although bone deformities such as shortness of neck and vertebrae, kyphosis, scoliosis, pectus carinatum, genu varum or valgum are frequent, association with osteopenia/osteoporosis has been rarely reported. Although spondyloepiphyseal dysplasia tarda and osteopenia are coexisting in the literature, there is no evidence of the association of spondyloepiphyseal dysplasia tarda and conjunctiva with osteoporosis. In our case report, we presented a patient who was applied to our center with short stature, diagnosed with osteoporosis and spondyloepiphyseal dysplasia congenita by detecting femur head aplasia in radiological imaging.
dc.identifier.doi10.4274/tod.37167
dc.identifier.endpage118
dc.identifier.issn2146-3816
dc.identifier.issue3
dc.identifier.startpage115
dc.identifier.urihttps://doi.org/10.4274/tod.37167
dc.identifier.urihttps://turkosteoporozdergisi.org/articles/doi/tod.37167
dc.identifier.urihttps://hdl.handle.net/11452/46449
dc.identifier.volume23
dc.identifier.wos000437429200008
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherGalenos Yayıncılık
dc.relation.journalTürk Osteoporoz Dergisi-Turkish Journal of Osteoporosis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectProgressive pseudorheumatoid dysplasia
dc.subjectCol2a1
dc.subjectTarda
dc.subjectGene
dc.subjectOsteoporosis
dc.subjectSpondyloepiphyseal dysplasia
dc.subjectSkeletal dysplasia
dc.subjectRheumatology
dc.titleAn uncommon reason of osteoporosis: Spondyloepiphyseal dysplasia congenita
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı/Endokrinoloji ve Metabolizma Hastalıkları Bilim Dalı
local.indexed.atWOS
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relation.isAuthorOfPublication.latestForDiscovery4ebb27f5-06de-45b8-8773-ea3452507df3

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