Cowden Syndrome: Case Report, Update and Proposed Diagnostic and Surveillance Routines

Cowden syndrome (CS) is an infrequent autosomal dominant multisystem genodermatosis, generally involving the skin, oral mucosa, thyroid, breast and gastrointestinal tract. It is characterized by a late onset in the 2(nd) or 3(rd) decade of life, an extraordinary potential for malignant transformatio...

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Detalles Bibliográficos
Autores principales: Molvi, Masuma, Sharma, Yugal K, Dash, Kedarnath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Special Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458935/
https://www.ncbi.nlm.nih.gov/pubmed/26120150
http://dx.doi.org/10.4103/0019-5154.156360

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458935/
https://www.ncbi.nlm.nih.gov/pubmed/26120150
http://dx.doi.org/10.4103/0019-5154.156360

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