Gorlin Syndrome
- PMID: 28613671
- Bookshelf ID: NBK430921
Gorlin Syndrome
Excerpt
Gorlin syndrome, also called Gorlin-Goltz syndrome, basal cell nevus syndrome (BCNS), or nevoid basal cell carcinoma syndrome, is an autosomal dominant familial cancer syndrome. It is characterized by numerous basal cell carcinomas (BCCs), along with skeletal, ophthalmologic, and neurologic abnormalities. Multiple neoplasms arise starting in childhood.
Copyright © 2025, StatPearls Publishing LLC.
Conflict of interest statement
Sections
References
-
- Hazemann G, Michel C, Mahé A, Lipsker D, Cribier B. [Histopathological study of basaloid follicular hamartoma]. Ann Dermatol Venereol. 2019 Mar;146(3):181-191. - PubMed
-
- Hasan A, Akintola D. An Update of Gorlin-Goltz Syndrome. Prim Dent J. 2018 Sep 01;7(3):38-41. - PubMed
-
- Gianferante DM, Rotunno M, Dean M, Zhou W, Hicks BD, Wyatt K, Jones K, Wang M, Zhu B, Goldstein AM, Mirabello L. Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data. Mol Genet Genomic Med. 2018 Nov;6(6):1168-1180. - PMC - PubMed
-
- Shevchenko A, Durkin JR, Moon AT. Generalized basaloid follicular hamartoma syndrome versus Gorlin syndrome: A diagnostic challenge. Pediatr Dermatol. 2018 Nov;35(6):e396-e397. - PubMed
Publication types
LinkOut - more resources
Full Text Sources