Basal Cell Carcinomas in Gorlin Syndrome: A Review of 202 Patients

Gorlin syndrome (Naevoid Basal Cell Carcinoma Syndrome) is a rare autosomal dominant syndrome caused by mutations in the PTCH gene with a birth incidence of approximately 1 in 19,000. Patients develop multiple basal cell carcinomas of the skin frequently in early life and also have a predisposition...

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Detalles Bibliográficos
Autores principales: Jones, Elizabeth A., Sajid, Mohammed Imran, Shenton, Andrew, Evans, D. Gareth
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998699/
https://www.ncbi.nlm.nih.gov/pubmed/21152126
http://dx.doi.org/10.1155/2011/217378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998699/
https://www.ncbi.nlm.nih.gov/pubmed/21152126
http://dx.doi.org/10.1155/2011/217378

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