Greig Cephalopolysyndactyly Syndrome with Oral Manifestations: A Rare Case Report

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 syndact...

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Detalles Bibliográficos
Autores principales: Unni, Jiji V, Daryani, Deepak, Sreejan, K C, Uthkal, P M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289203/
https://www.ncbi.nlm.nih.gov/pubmed/32566533
http://dx.doi.org/10.4103/ijabmr.IJABMR_391_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289203/
https://www.ncbi.nlm.nih.gov/pubmed/32566533
http://dx.doi.org/10.4103/ijabmr.IJABMR_391_18

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