International Journal of Applied and Basic Medical Research

CASE REPORT
Year
: 2020  |  Volume : 10  |  Issue : 2  |  Page : 140--142

Greig cephalopolysyndactyly syndrome with oral manifestations: A rare case report


Jiji V Unni, Deepak Daryani, KC Sreejan, PM Uthkal 
 Department of Oral Medicine and Radiology, Malabar Dental College and Research Centre, Edappal, Kerala, India

Correspondence Address:
Jiji V Unni
Department of Oral Medicine and Radiology, Malabar Dental College and Research Centre, Edappal, Kerala
India

Greig cephalopolysyndactyly syndrome (GCPS) is one of the autosomal dominant-inherited syndromes, caused by haploinsufficiency of the GLI3 gene. It is a rare, multiple congenital syndrome with an estimated rate of 0.009%. With the classic clinical triad of preaxial polydactyly with cutaneous syndactyly of at least one limb, hypertelorism, and macrocephaly, presumptive diagnosis of GCPS is made. The purpose of this article is to report a case of GCPS with emphasis on craniofacial and oral features.


How to cite this article:
Unni JV, Daryani D, Sreejan K C, Uthkal P M. Greig cephalopolysyndactyly syndrome with oral manifestations: A rare case report.Int J App Basic Med Res 2020;10:140-142


How to cite this URL:
Unni JV, Daryani D, Sreejan K C, Uthkal P M. Greig cephalopolysyndactyly syndrome with oral manifestations: A rare case report. Int J App Basic Med Res [serial online] 2020 [cited 2021 Jan 22 ];10:140-142
Available from: https://www.ijabmr.org/article.asp?issn=2229-516X;year=2020;volume=10;issue=2;spage=140;epage=142;aulast=Unni;type=0