Early onset Peutz–Jeghers syndrome, the importance of appropriate diagnosis and follow-up: A case report

RATIONALE: Peutz–Jeghers syndrome (PJS) is currently defined as an inherited condition, also called a familial hamartomatous polyposis syndrome, characterized by the association between pigmented mucocutaneous lesions and hamartomatous polyps in the gastrointestinal tract, especially in the small bo...

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Detalles Bibliográficos
Autores principales: Mărginean, Cristina Oana, Meliţ, Lorena Elena, Patraulea, Florin, Iunius, Simu, Mărginean, Maria Oana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635162/
https://www.ncbi.nlm.nih.gov/pubmed/31277194
http://dx.doi.org/10.1097/MD.0000000000016381

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635162/
https://www.ncbi.nlm.nih.gov/pubmed/31277194
http://dx.doi.org/10.1097/MD.0000000000016381

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