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Komar D
Publications
Audiological Diagnostics and Treatment of Craniofacial Abnormalities in Cleidocranial Dysplasia CCD
Introduction: Cleidocranial dysplasia CCD is a rare genetic disorder connected with mutation in the gene RUNX2. The characteristic feature of this syndrome is a triad of symptoms: hypoplasia or aplasia of clavicles, cranial defects, persistent decidous teeth and multiple supernumerary teeth with consecutive failure in succedaneous teeth eruption. O... Read More»
Renata Turska-Malińska, Matthews-Brzozowska T, Hojan-Jezierska D and Komar D
Case Report: J Interdiscipl Med Dent Sci 2017, 5: 2
DOI: 10.4172/2376-032X.1000210
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