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Peutz-Jeghers syndrome: Four cases in one family
Peutz-Jeghers syndrome (PJS) is a rare, but life-threatening, familial inherited disease, characterized by mucocutaneous pigmentation and hamartomatous polyps. The estimated incidence of PJS ranges from 1/50,000 to 1/200,000. PJS can significantly increase the risk of malignancies, and especially ga...
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| Publicado no: | Intractable Rare Dis Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4761583/ https://ncbi.nlm.nih.gov/pubmed/26989648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2015.01036 |
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