A Case Report on Cleidocranial Dysplasia: Diagnosis and Treatment

We attending in report a case of CCD that was not previously diagnosed by way of the extremely depressed incidence of this disorder.A exceptional congenital autosomal main skeletal disorder called cleidocranial dysplasia (CCD) influences the skull. Human RUNX2, that can be found on the short arm of deoxyribonucleic acid 6p21, has heterozygosity of mutations that cause the disorder. One per million live births is the occurrence of CCD. About 40% of patients with the condition knowledge spontaneous attack of CCD, and one in three of these patients has unchanged parents. The most prevalent face associated with CCD are aplastic or hypoplastic clavicles, excessive teeth, failed ejection of permanent dentition, and a hypoplastic maxilla.A 13-year-traditional Caucasian boy was refer to the ortho- dontic clinic of the School of Dentistry, Aristotle University, Thessaloniki, Greece. The patient was subsequently pinpointed with CCD established the clinical examination, sweeping X-ray, anterior-posterior and sideways cephalogram, and chest radiograph verdicts. The details of this case are within reported by way of the extremely low occurrence of this disorder. The overall situation goal is to enact functional occlu-sion and an beautiful facial and dental appearance.Sometimes this disorder causes cognitive problems for the cases; therefore, proper ambition and sup- traffic are important.

Author(s) Details:

Olga-Elpis Kolokitha,
Department of Orthodontics, School of Dentistry, Aristotle University of Thessaloniki, Thessaloniki, GR -54124, Greece.

Ioulia Ioannidou,
Department of Orthodontics, School of Dentistry, Aristotle University of Thessaloniki, Thessaloniki, GR -54124, Greece.

Please see the link here: https://stm.bookpi.org/PRAMR-V12/article/view/9661

Keywords: Cleidocranial dysplasia, delayed eruption, supernumerary teeth