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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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Dades bibliogràfiques
Autors principals: Taheri, Diana, Afshar-Moghadam, Noushin, Mahzoni, Parvin, Eftekhari, Amin, Hashemi, Seyed Mozafar, Emami, Mohammad Hasan, Fesharakizadeh, Mehdi, Ghasemi-basir, Hamid Reza
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2013
Matèries:
Accés en línia: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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