A Pediatric Case of Cowden Syndrome with Graves' Disease

Cowden syndrome (CS) is a rare dominantly inherited multisystem disorder, characterized by an extraordinary malignant potential. In 80% of cases, the human tumor suppressor gene phosphatase and tensin homolog (PTEN) is mutated. We present a case of a 17-year-old boy with genetically confirmed CS and...

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Detalles Bibliográficos
Autores principales: Patraquim, Cláudia, Fernandes, Vera, Martins, Sofia, Antunes, Ana, Marques, Olinda, Carvalho, José Luís, Correia-Pinto, Jorge, Meireles, Carla, Ferreira, Ana Margarida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306985/
https://www.ncbi.nlm.nih.gov/pubmed/28251007
http://dx.doi.org/10.1155/2017/2750523

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306985/
https://www.ncbi.nlm.nih.gov/pubmed/28251007
http://dx.doi.org/10.1155/2017/2750523

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