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Gorlin syndrome: A rare case report

Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in PTCH, a tumor suppressor gene that has been mapped to chromosome 9q22.3-q31. It is observed that most aggressive forms of keratocystic odontoge...

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Detalles Bibliográficos
Autores principales: Shrivastava, Sandhya, Nayak, Sushruth, Nayak, Prachi, Sahu, Sourabh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083426/
https://www.ncbi.nlm.nih.gov/pubmed/33967525
http://dx.doi.org/10.4103/0973-029X.190048