Frameshift mutation in exon 17 of PTCH1 gene in Nevoid basal cell carcinoma syndrome: A case report

Nevoid basal cell carcinoma syndrome (NBCCS) is a rare autosomal dominant disorder characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. In majority of the cases, the presence of multiple and recurrent jaw cysts especially during the first two decades of lif...

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Detalles Bibliográficos
Autores principales: Aravind, Thara, Savithri, Vindhya, Suresh, Rakesh, Subash, Pramod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112701/
https://www.ncbi.nlm.nih.gov/pubmed/37082289
http://dx.doi.org/10.4103/jomfp.jomfp_463_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112701/
https://www.ncbi.nlm.nih.gov/pubmed/37082289
http://dx.doi.org/10.4103/jomfp.jomfp_463_20

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