Cleidocranial Dysplasia Affecting Three Generations in a Family: A Unique Case Report

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,...

Full description

Bibliographic Details

Published in:	Journal of Krishna Institute of Medical Sciences University
Main Authors:	Vathsala Patil, Keerthilatha M. Pai, Yogesh Chhaparwal, Shubha Chhaparwal
Format:	Article
Language:	English
Published:	Krishna Vishwa Vidyapeeth (Deemed to be University), Karad 2021-04-01
Subjects:	cleidocranial dysplasia familial supernumerary teeth
Online Access:	https://www.jkimsu.com/jkimsu-vol10no2/JKIMSU,%20Vol.%2010,%20No.%202,%20April-June%202021%20Page%20150-155.pdf