Cleidocranial Dysplasia: Case Report
Özet
A 31-year-old man experienced bilateral posterior glenohumeral dislocation during seizures. He had cleidocranial dysplasia with complete absence of both clavicles. Cleidocranial dysplasia is a rare inherited disease also known as Marie-Sainton syndrome and responsible for dental abnormalities well-known to stomatologists and dentists. Other manifestations include defective development of the skull bones and hypoplastic or aplastic clavicles. We found no previous reports of bilateral posterior glenohumeral dislocation in patients with cleidocranial dysplasia. The objective of this work was to look for an association between clavicular aplasia and posterior glenohumeral dislocation. (C) 2015 Elsevier Masson SAS. All rights reserved.
Anahtar kelimeler
Atıf için künye
BİLGE, N. H., BAYRAKDAR, İ. Ş., AZLAĞ PEKİNCE, K., & Çağlayan, F. (2015). Cleidocranial Dysplasia: Case Report. Turkiye Klinikleri Journal of Dental Sciences Cases, 1, 159–162. https://doi.org/10.5336/dentalcase.2015-43632
BibTeX
@article{bilge2015-9972,
author = {BİLGE, Nebiha Hilal and BAYRAKDAR, İBRAHİM ŞEVKİ and AZLAĞ PEKİNCE, KADER and Çağlayan, Fatma},
title = {Cleidocranial Dysplasia: Case Report},
journal = {Turkiye Klinikleri Journal of Dental Sciences Cases},
year = {2015},
volume = {1},
pages = {159--162},
issn = {2149-3375},
doi = {10.5336/dentalcase.2015-43632},
url = {https://akademik.atauni.edu.tr/yayinlar/9972-cleidocranial-dysplasia-case-report}
}