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Squamous cell carcinoma arising in familial gingival fibromatosis—a rare case report
Familial gingival fibromatosis is a rare hereditary condition due to chromosomal abnormality which can occur as an isolated disease or as part of a syndrome and has an incidence of 1:350 000. This condition leads to esthetic, functional, psychological and masticatory disturbance of the oral cavity....
Tallennettuna:
| Julkaisussa: | J Surg Case Rep |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5633648/ https://ncbi.nlm.nih.gov/pubmed/29026519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jscr/rjx197 |
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