Cancer problem in Peutz–Jeghers syndrome

Peutz–Jeghers syndrome is a rare autosomal dominantly inherited condition, characterized by the presence of hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome can be associated with other neoplasms such as ovarian neoplasms known as sex-cord tumor with...

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Detalles Bibliográficos
Autores principales: Taheri, Diana, Afshar-Moghadam, Noushin, Mahzoni, Parvin, Eftekhari, Amin, Hashemi, Seyed Mozafar, Emami, Mohammad Hasan, Fesharakizadeh, Mehdi, Ghasemi-basir, Hamid Reza
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/PMC3748667/
https://www.ncbi.nlm.nih.gov/pubmed/23977663
http://dx.doi.org/10.4103/2277-9175.109721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748667/
https://www.ncbi.nlm.nih.gov/pubmed/23977663
http://dx.doi.org/10.4103/2277-9175.109721

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