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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer Health
2019
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| Materias: | |
| 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 |