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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
Main Authors: Taheri, Diana, Afshar-Moghadam, Noushin, Mahzoni, Parvin, Eftekhari, Amin, Hashemi, Seyed Mozafar, Emami, Mohammad Hasan, Fesharakizadeh, Mehdi, Ghasemi-basir, Hamid Reza
Formato: Artigo
Idioma:Inglês
Publicado: Medknow Publications & Media Pvt Ltd 2013
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3748667/
https://ncbi.nlm.nih.gov/pubmed/23977663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.109721
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