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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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| Vydáno v: | Medicine (Baltimore) |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer Health
2019
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| Témata: | |
| On-line přístup: | 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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