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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,...

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Bibliografische gegevens
Hoofdauteurs: Vathsala Patil, Keerthilatha M. Pai, Yogesh Chhaparwal, Shubha Chhaparwal
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Krishna Vishwa Vidyapeeth (Deemed to be University), Karad 2021-04-01
Reeks:Journal of Krishna Institute of Medical Sciences University
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Online toegang:https://www.jkimsu.com/jkimsu-vol10no2/JKIMSU,%20Vol.%2010,%20No.%202,%20April-June%202021%20Page%20150-155.pdf
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