First Polish Cowden syndrome patient with confirmed PTEN gene mutation

Cowden syndrome is a rare hereditary disease. Incidence of the disease is conditioned by occurrence of mutations in the PTEN gene. The disease has a frequency of 1/120,000 newborn and it predisposes to the occurrence of hamartoma polyps in the gastrointestinal tract, skin tumours, as well as tumours...

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Detalles Bibliográficos
Autores principales: Podralska, Marta, Nowakowska, Dorota, Steffen, Jan, Cichy, Wojciech, Slomski, Ryszard, Plawski, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278958/
https://www.ncbi.nlm.nih.gov/pubmed/22371735
http://dx.doi.org/10.5114/aoms.2010.13522

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278958/
https://www.ncbi.nlm.nih.gov/pubmed/22371735
http://dx.doi.org/10.5114/aoms.2010.13522

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