Cowden syndrome- Clinico-radiological illustration of a rare case

Cowden syndrome (CS) or multiple hamartoma syndrome is an infrequent genodermatoses, which is inherited as an autosomal dominant trait resulting from the mutation in the Phosphatase and Tensin homolog gene on the arm 10q and is principally characterized by multiple hamartomas with an increased risk...

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Detalles Bibliográficos
Autores principales: Patil, Prashant B., Sreenivasan, V., Goel, Sumit, Nagaraju, K., Vashishth, Shirin, Gupta, Swati, Garg, Kanika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703684/
https://www.ncbi.nlm.nih.gov/pubmed/23853470
http://dx.doi.org/10.4103/0976-237X.111634

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703684/
https://www.ncbi.nlm.nih.gov/pubmed/23853470
http://dx.doi.org/10.4103/0976-237X.111634

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