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

Greig cephalopolysyndactyly syndrome with oral manifestations: A rare case report


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
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijabmr.IJABMR_391_18

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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.


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