Abstract

Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximately 1 per million individuals worldwide. This syndrome is characterized by skeletal, orofacial, and dental manifestations like hypoplastic or aplastic clavicle, shoulder hypermobility, patent or delayed closure of fontanelles, and multiple impacted supernumerary teeth with delayed eruption pattern. Early diagnosis and management with a comprehensive team approach are crucial for an overall better prognosis. In this paper, we describe three generations of cleidocranial dysplasia presented in the same family with their clinical features and treatment strategies.

Original languageEnglish
Pages (from-to)150-155
Number of pages6
JournalJournal of Krishna Institute of Medical Sciences University
Volume10
Issue number2
Publication statusPublished - 01-04-2021

All Science Journal Classification (ASJC) codes

  • General Medicine

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