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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Kalogeropoulou, Christina, Zampakis, Petros, Kazantzi, Santra, Kraniotis, Pantelis, Mastronikolis, Nicholas S
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2009
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2803884/
https://ncbi.nlm.nih.gov/pubmed/20062724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-2-9087
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker