Cleidocranial Dysplasia: Case Report


BİLGE N. H., BAYRAKDAR İ. Ş., AZLAĞ PEKİNCE K., ÇAĞLAYAN F.

Turkiye Klinikleri Journal of Dental Sciences Cases, cilt.1, ss.159-162, 2015 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1
  • Basım Tarihi: 2015
  • Doi Numarası: 10.5336/dentalcase.2015-43632
  • Dergi Adı: Turkiye Klinikleri Journal of Dental Sciences Cases
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.159-162
  • Anahtar Kelimeler: Clavicular agenesis, Bilateral posterior glenohumeral dislocation, Cleidocranial dysplasia
  • Atatürk Üniversitesi Adresli: Evet

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.