Delayed diagnosis of Gorlin syndrome: Learning from mistakes!

Gorlin syndrome (GS) is a rare inherited multisystem disorder with predisposition to basal cell carcinomas and various other neoplasms. Characteristic features include falx calcification, multiple odontogenic keratocysts (OKCs), early onset medulloblastoma, craniofacial and skeletal malformations, c...

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Detalles Bibliográficos
Autores principales: Ramanathan, Subramaniyan, Kumar, Devendra, Al Heidous, Mahmoud, Palaniappan, Yegu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770649/
https://www.ncbi.nlm.nih.gov/pubmed/26962343
http://dx.doi.org/10.4103/1817-1745.174437

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770649/
https://www.ncbi.nlm.nih.gov/pubmed/26962343
http://dx.doi.org/10.4103/1817-1745.174437

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