Cleidocranial Dysplasia: A Case Report

Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease. CCD is caused by mutation in the gene on 6p21 encoding transcription factor CBFA1, i.e. runt−related transcription factor 2(RUNX2). The disease is characterized by a persistently open anterior fontanelle and skull sutures,...

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Bibliografski detalji
Glavni autori: Karagüzel, Gülay, Aktürk, Filiz Azar, Okur, Emelgül, Gümele, Halit Reşit, Gedik, Yusuf, Ökten, Ayşenur
Format: Artigo
Jezik:Inglês
Izdano: Galenos Publishing 2010
Teme:
Case Reports
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3005677/
https://ncbi.nlm.nih.gov/pubmed/21274329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.v2i3.134
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