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Osteopoıkılosıs at Hand And Foot Fıngers: Case Report

ArticleYayıncıda açık erişim

Özet

Osteopoikilosis is a rare and genetical benign bone disease which is not well defined in terms of its phenotypic characteristics. In literature, it is generally stated that it holds large and medium bone metaphyses and phenotypic features are not mentioned. We will also notice that our patients can also retain small bone metaphyses and have typical phenotypic features.

Anahtar Kelimeler

Patoloji
RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/22479Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.30565/medalanya.396291Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorÇamurcu, İsmet Yalkın
dc.contributor.authorÖzcan, Seçkin
dc.contributor.authorAltay, Rıdvan
dc.date.accessioned2026-10-20T11:09:40.129248040Z
dc.date.available2026-10-20T11:09:40.129248040Z
dc.date.issued2018
dc.description.abstractOsteopoikilosis is a rare and genetical benign bone disease which is not well defined in terms of its phenotypic characteristics. In literature, it is generally stated that it holds large and medium bone metaphyses and phenotypic features are not mentioned. We will also notice that our patients can also retain small bone metaphyses and have typical phenotypic features.
dc.identifier.doi10.30565/medalanya.396291
dc.identifier.eissn2587-0319
dc.identifier.endpage130
dc.identifier.issue2
dc.identifier.startpage127
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/22479
dc.identifier.volume2
dc.language.isotr
dc.relation.ispartofActa Medica Alanya
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPatoloji
dc.titleOsteopoıkılosıs at Hand And Foot Fıngers: Case Report
dc.typeArticle
dspace.entity.typePublication
rdl.citation.trdizin0
rdl.oa.statusgold
rdl.oa.urlhttps://dergipark.org.tr/en/download/article-file/500558
rdl.source.indexTRDIZIN