Early Diagnosis and Intervention in Familial Nevoid Basal Cell Carcinoma Syndrome: A Case Report of Generational Surveillance
Year: 2025
Type: article
Abstract: Introduction Familial Nevoid Basal Cell Carcinoma Syndrome (FNBCC), also known as Gorlin syndrome. The syndrome, delineated by Gorlin and Goltz in 1960 was first reported in 1894(1), is a rare autosomal dominant genetic disorder characterized by a heterogeneous array of clinical manifestations affecting multiple organ systems. Gorlin and Goltz defined the condition as a syndrome comprising the principal triad of multiple basal cell nevi, jaw keratocystic odontogenic tumors, and skeletal anomalies (2)
Author: International Journal of Dental Science and Innovative Research (IJDSIR)
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W6912000313
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