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A case report of hamartomatous polyposis in an individual with Neurofibromatosis type 1
Even in well‐described genetic syndromes, such as neurofibromatosis type 1, expansion of the phenotype should be considered as a possible explanation for atypical presentations. However, it is critical to complete the evaluation for a potential dual diagnosis, as there could be significant prognosti...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333055/ https://www.ncbi.nlm.nih.gov/pubmed/30656042 http://dx.doi.org/10.1002/ccr3.1908 |