Gorlin-Goltz syndrome: incidental finding on routine ct scan following car accident

INTRODUCTION: Gorlin-Goltz syndrome is a rare hereditary disease. Pathogenesis of the syndrome is attributed to abnormalities in the long arm of chromosome 9 (q22.3-q31) and loss or mutations of human patched gene (PTCH1 gene). Multiple basal cell carcinomas (BCCs), odontogenic keratocysts, skeletal...

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Detalles Bibliográficos
Autores principales: Kalogeropoulou, Christina, Zampakis, Petros, Kazantzi, Santra, Kraniotis, Pantelis, Mastronikolis, Nicholas S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803884/
https://www.ncbi.nlm.nih.gov/pubmed/20062724
http://dx.doi.org/10.1186/1757-1626-2-9087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803884/
https://www.ncbi.nlm.nih.gov/pubmed/20062724
http://dx.doi.org/10.1186/1757-1626-2-9087

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