CLEIDOCRANIAL DYSPLASIA: A CASE REPORT

Authors

  • Fizza Tahir CMH Lahore Medical College, Lahore Pakistan
  • Maila Habib Piracha CMH Lahore Medical College, Lahore Pakistan
  • Fatima Hafeez CMH Lahore Medical College, Lahore Pakistan
  • Samman Hassan 1CMH Lahore Medical College, Lahore Pakistan
  • Hira Butt Sharif Medical and Dental College, Lahore Pakistan
  • Nayyab Rauf CMH Lahore Medical College, Lahore Pakistan

Abstract

Cleidocranial dysplasia (CCD) also known by the name of Marie and Sainton‘s disease, is a rare autosomal dominant disease characterized by multiple skeletal and dental anomalies. This case report presents a 21-year-old male patient with short stature, hypoplastic clavicles, patent anterior fontanels, maxillary hypoplasia, hypertelorism, parietal and occipital bossing, retained deciduous and supernumerary teeth. On the basis of clinical and radiographic findings the patient was diagnosed with CCD. The details of the case are reported herein because of the extremely low incidence of this disorder. Early diagnosis is crucial as it helps in better management of dental anomalies to improve quality of life. The dental management of Cleidocranial Dysplasia demands a multidisciplinary approach with Surgical, Orthodontic and Prosthodontic expertise to improve function and aesthetics.

Key Words: Cleidocranial dysplasia, Hypoplastic clavicles, Dental anomalies.

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Published

30-06-2021

How to Cite

1.
Tahir F, Piracha MH, Hafeez F, Hassan S, Butt H, Rauf N. CLEIDOCRANIAL DYSPLASIA: A CASE REPORT. Pak J Pathol [Internet]. 2021 Jun. 30 [cited 2024 Dec. 22];32(2):79-81. Available from: https://pakjpath.com/index.php/Pak-J-Pathol/article/view/655

Issue

Vol. 32 No. 2 (2021): Pakistan Journal of Pathology

Section

Case Report

License

Copyright (c) 2021 Fizza Tahir, Maila Habib Piracha, Fatima Hafeez, Samman Hassan, Hira Butt, Nayyab Rauf

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