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Osteopoıkılosıs at Hand And Foot Fıngers: Case Report

ArticleAçık 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/20064Resmi 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.accessioned2026-10-18T21:12:00.020739863Z
dc.date.available2026-10-18T21:12:00.020739863Z
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/20064
dc.identifier.volume2
dc.language.isotr
dc.relation.ispartofActa Medica Alanya
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPatoloji
dc.titleOsteopoıkılosıs at Hand And Foot Fıngers: Case Report
dc.typeArticle
dspace.entity.typePublication
rdl.citation.trdizin0
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.source.indexTRDIZIN