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Audiological Diagnostics and Treatment of Craniofacial Abnormalities in Cleidocranial Dysplasia CCD | OMICS International | Abstract
ISSN: 2376-032X

JBR Journal of Interdisciplinary Medicine and Dental Science
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Case Report

Audiological Diagnostics and Treatment of Craniofacial Abnormalities in Cleidocranial Dysplasia CCD

Turska-Malińska R1*, Matthews-Brzozowska T1, Hojan-Jezierska D2 and Komar D2

1Department of Maxillofacial Orthopedics and Orthodontics, Poznan Medical University, Poland

2Biophysics Department of Hearing Healthcare Profession Poznan Medical University, Poland

*Corresponding Author:
Dr. Renata Turska-Malińska
Chair and Department of Maxillofacial Orthopedics and Orthodontics
Poznan Medical University, Poland
Tel: +0048 507110530
E-mail: renata.turska.malinska@wp.pl

Received Date: April 20, 2017; Accepted Date: April 24, 2017; Published Date: April 30, 2017

Citation: Malinska T, Brzozowska M, Jezierska H, Komar D (2017) Audiological Diagnostics and Treatment of Craniofacial Abnormalities in Cleidocranial Dysplasia CCD. J Interdiscipl Med Dent Sci 5: 210. doi:10.4172/2376-032X.1000210

Copyright: © 2017 Renata Turska-Malińska, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

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. Objective: The aim of the study is to present a CCD patient, in which during orthodontic treatment there was performed a comprehensive hearing test. Case report: The paper presents a 15-year-old patient in whom intraorally there were stated only 4 first permanent molars and 1 lower central incisor while all the remaining teeth were decidous. The CBCT showed 11 impacted supernumerary teeth. Treatment started by surgical exposure and orthodontic traction of the upper incisors into the arch. The introduced fixed appliance seems to be a good solution to pull down impacted anterior teeth. An audiological examination of the patient with CCD revealed normal hearing on the border of norm, however tympanometry may suggest a defect of the auditory ossicles. Conclusion: Active long-term treatment that requires cooperation of many specialists is the correct procedure in CCD cases.

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