Gorlin-Goltz Syndrome: Case Report of a Rare Hereditary Disorder

Introduction. Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. Case Report. The present paper highlights the importance of diagnostic criteria and histopathology in early and prompt diagnosis which will lead to proper treat...

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Detalles Bibliográficos
Autores principales: Agrawal, Ashutosh, Murari, Aditi, Vutukuri, Sunil, Singh, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461617/
https://www.ncbi.nlm.nih.gov/pubmed/23050170
http://dx.doi.org/10.1155/2012/475439

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461617/
https://www.ncbi.nlm.nih.gov/pubmed/23050170
http://dx.doi.org/10.1155/2012/475439

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