TY - JOUR
T1 - Cleidocranial dysplasia affecting three generations in a family
T2 - A unique case report
AU - Patil, Vathsala
AU - Pai, Keerthilatha M.
AU - Chhaparwal, Yogesh
AU - Chhaparwal, Shubha
N1 - Publisher Copyright:
© Journal of Krishna Institute of Medical Sciences University.
PY - 2021/4/1
Y1 - 2021/4/1
N2 - 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.
AB - 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.
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M3 - Article
AN - SCOPUS:85111051344
SN - 2231-4261
VL - 10
SP - 150
EP - 155
JO - Journal of Krishna Institute of Medical Sciences University
JF - Journal of Krishna Institute of Medical Sciences University
IS - 2
ER -