Dermatol. praxi. 2022;16(1):45-47 | DOI: 10.36290/der.2022.008

Gorlin-Goltz syndrome - case report

MUDr. Martina Blažková
Kožní oddělení, Nemocnice Jihlava

Gorlin-Goltz syndrome or basal cell nevus syndrome is a rare genetically inherited disease. Most imortant skin manifestation are multiple basal cell carcinomas in a young age or even in a childhood. Gorlin-Goltz syndrome is connected with multiple comorbidities. In our case report we describe 27-years old men with a presence of multiple basal cell carcinomas, history of odontogenic keratocysts, facial abnormalities and calcification of meninges. Multidisciplinary dispensarisation has been provided since a confirmation of diagnosis.

Keywords: Gorlin-Goltz syndrome, basal cell carcinoma, guidelines.

Published: April 4, 2022  Show citation

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Blažková M. Gorlin-Goltz syndrome - case report. Dermatol. praxi. 2022;16(1):45-47. doi: 10.36290/der.2022.008.
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References

  1. Verkouteren BJA, Cosgun B, Reinders MGHC, et al. A guideline for the clinical management of basal cell naevus syndrome (Gorlin-Goltz syndrome). Br J Dermatol. 2021;186(2): 215-226. https://doi.org/10.1111/bjd.20700. Go to original source... Go to PubMed...
  2. Bree AF, Shah MR. BCNS Colloquium Group. Consensus statement from the first international colloquium on basal cell nevus syndrome (BCNS). Am J Med Genet A. 2011;155A(9):2091-2097. Go to original source... Go to PubMed...
  3. Jawa DS, Sircar K, Somani R, Grover N, Jaidka S, Singh S. Gorlin-Goltz syndrome. J Oral Maxillofac Pathol. 2009;13(2):89-92. doi: 10.4103/0973-029X.57677. Go to original source... Go to PubMed...
  4. Moramarco A, Himmelblau E, Miraglia E, et al. Ocular manifestations in Gorlin-Goltz syndrome. Orphanet J Rare Dis. 2019;14(218) https://doi.org/10.1186/s13023-019-1190-1196. Go to original source... Go to PubMed...
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