Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1960 1
1963 1
1972 1
1973 1
1974 1
1975 4
1976 1
1977 4
1978 2
1979 4
1980 2
1981 2
1982 4
1983 3
1984 3
1985 7
1986 5
1987 5
1988 3
1989 5
1990 6
1991 7
1992 3
1993 3
1994 3
1995 5
1996 2
1997 4
1998 3
1999 4
2000 7
2001 3
2002 5
2003 5
2004 11
2005 3
2006 7
2007 12
2008 7
2009 13
2010 15
2011 17
2012 14
2013 22
2014 34
2015 29
2016 26
2017 16
2018 20
2019 17
2020 22
2021 24
2022 30
2023 25
2024 24
2025 23
2026 16

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

497 results

Results by year

Filters applied: . Clear all
Page 1
Prenatal detection of Gorlin-Goltz syndrome: a case report and focused review of the literature.
Oelmeier K, Horváth J, Vogtmann R, Meyer-Wittkopf M, Möllers M, Schmitz R, Oberste KM, Willy D. Oelmeier K, et al. Front Med (Lausanne). 2026 Apr 1;13:1659100. doi: 10.3389/fmed.2026.1659100. eCollection 2026. Front Med (Lausanne). 2026. PMID: 41994461 Free PMC article.
INTRODUCTION: Gorlin-Goltz syndrome is a rare tumor-predisposing condition caused by genetic variants in the PTCH1 and SUFU pathways. ...DISCUSSION: In the presence of typical prenatal features, this genetic variant was reclassified as likely pathogenic for …
INTRODUCTION: Gorlin-Goltz syndrome is a rare tumor-predisposing condition caused by genetic variants in the PTCH1 and …
Genetic Insight into Gorlin-Goltz Syndrome.
Madhu M. Madhu M. Indian J Dermatol. 2026 Mar-Apr;71(2):87-93. doi: 10.4103/ijd.ijd_1165_23. Epub 2026 Feb 27. Indian J Dermatol. 2026. PMID: 41884741 Free PMC article.
Gorlin-Goltz syndrome, also called Basal cell nevus syndrome (BCNS), Nevoid basal cell carcinoma syndrome (NBCCS), or Basal nevus cell carcinoma syndrome (BNCCS) is a rare, inherited, autosomal dominant genodermatoses, with variable expre …
Gorlin-Goltz syndrome, also called Basal cell nevus syndrome (BCNS), Nevoid basal cell carcinoma syndrome …
Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study.
Liu L, Du H, Wang N, Lv S, Yu C, Deng L. Liu L, et al. Front Med (Lausanne). 2026 Feb 24;13:1778460. doi: 10.3389/fmed.2026.1778460. eCollection 2026. Front Med (Lausanne). 2026. PMID: 41816662 Free PMC article.
Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome) is a rare autosomal dominant tumor-predisposition disorder characterized by multiple basal cell carcinomas (BCCs), odontogenic keratocysts of the jaws, and variable systemic manifestations. . …
Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome) is a rare autosomal dominant tumor-predisposition d …
Report of Concomitant Intracranial Cysts in Unrelated Patients With Heterozygous Germline NF1 Pathogenic Variants.
Harahsheh EY, Merritt E, Tejon JB, Olarewaju BA, Asif MB, Babovic-Vuksanovic D, Osundiji MA. Harahsheh EY, et al. Ann Intern Med Clin Cases. 2026 Feb;5(2):e250802. doi: 10.7326/aimcc.2025.0802. Epub 2026 Feb 3. Ann Intern Med Clin Cases. 2026. PMID: 41696550 Free PMC article.
Although odontogenic cysts are well known to be associated with Gorlin-Goltz syndrome, the possibilities of other genetic disorders in patients with odontogenic and other intracranial cystic lesions have continued to stir research interests. ...
Although odontogenic cysts are well known to be associated with Gorlin-Goltz syndrome, the possibilities of other genet …
Successful Alternative Administration of Sonidegib in a Patient with Gorlin-Goltz Syndrome and Dysphagia: A Case Report.
Bender A, Krönig L. Bender A, et al. Case Rep Dermatol. 2025 Dec 8;18(1):96-101. doi: 10.1159/000546383. eCollection 2026 Jan-Dec. Case Rep Dermatol. 2025. PMID: 41668901 Free PMC article.
CONCLUSION: This case report describes the successful use of an alternative administration of sonidegib in a patient with Gorlin-Goltz syndrome and dysphagia....
CONCLUSION: This case report describes the successful use of an alternative administration of sonidegib in a patient with Gorlin-G …
Identification of a PORCN c.1093C>T (p.Arg365Trp) Variant in a 12-Year-Old Girl With Goltz-Gorlin Syndrome.
Bolzon A, Caroppo F, Passaglia L, Boaretto F, Salviati L, Belloni Fortina A. Bolzon A, et al. Clin Case Rep. 2026 Feb 2;14(2):e71592. doi: 10.1002/ccr3.71592. eCollection 2026 Feb. Clin Case Rep. 2026. PMID: 41641168 Free PMC article.
We report the first female case of Goltz-Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. ...
We report the first female case of Goltz-Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously …
Expanding the clinicopathological spectrum of nevoid basal cell carcinoma syndrome associated with odontogenic keratocyst in the Indian population: an institutional experience of 39 cases and review of the literature.
Bansal SP, Desai RS, Patil MS. Bansal SP, et al. Int J Oral Maxillofac Surg. 2026 May;55(5):532-541. doi: 10.1016/j.ijom.2025.12.008. Epub 2026 Jan 1. Int J Oral Maxillofac Surg. 2026. PMID: 41478811 Review.
Nevoid basal cell carcinoma syndrome (NBCCS) is a rare autosomal dominant hereditary condition associated with developmental abnormalities and tumourigenesis with a prevalence rate of 1:60,000. ...
Nevoid basal cell carcinoma syndrome (NBCCS) is a rare autosomal dominant hereditary condition associated with developmental abnormal …
Clinical relevance of the bifid ribs in humans.
Skrzat J, Popovchenko S. Skrzat J, et al. Folia Med Cracov. 2025 Jul 31;65(2):83-91. doi: 10.24425/fmc.2025.156126. Folia Med Cracov. 2025. PMID: 41329975 Free article. Review.
Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.
Yapijakis C, Ziakas N, Gintoni I, Papoulidis I, Vilos G, Chrousos GP. Yapijakis C, et al. Adv Exp Med Biol. 2026;1487:99-104. doi: 10.1007/978-3-032-03398-7_11. Adv Exp Med Biol. 2026. PMID: 41273553
INTRODUCTION: Gorlin syndrome (GS) or basal cell nevus syndrome type 1 (BCNS1) is a rare genetic disease belonging to the spectrum of genodermatoses. ...CONCLUSION: The suggested clinical diagnosis for Gorlin syndrome type 1 was confirmed by gen …
INTRODUCTION: Gorlin syndrome (GS) or basal cell nevus syndrome type 1 (BCNS1) is a rare genetic disease belonging to t …
497 results