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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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Detalhes bibliográficos
Publicado no:Medicine (Baltimore)
Main Authors: Mărginean, Cristina Oana, Meliţ, Lorena Elena, Patraulea, Florin, Iunius, Simu, Mărginean, Maria Oana
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Health 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6635162/
https://ncbi.nlm.nih.gov/pubmed/31277194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016381
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