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Peutz-Jeghers syndrome: Diagnostic and therapeutic approach
Peutz-Jeghers syndrome (PJS) is an inherited, autosomal dominant disorder distinguished by hamartomatous polyps in the gastrointestinal tract and pigmented mucocutaneous lesions. Prevalence of PJS is estimated from 1 in 8300 to 1 in 280 000 individuals. PJS predisposes sufferers to various malignanc...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The WJG Press and Baishideng
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2778095/ https://ncbi.nlm.nih.gov/pubmed/19916169 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.15.5397 |
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