Hereditary gingival fibromatosis: a case report
| Author | Gholam Ali Gholami | en |
| Author | Mohammad Mohammadi | en |
| Issued Date | 2013-09-03 | en |
| Abstract | Background: Hereditary gingival fibromatosis is a rare disease that could appear isolated or along with a syndrome. This disease is a dominant autosomal trait. The clinical appearance of this disease is in the form of nodular or symmetric. Malocclusion, diastema and delayed eruption of teeth are the other clinical signs of disease. | en |
| DOI | https://doi.org/ | en |
| Keyword | Fibromatosis | en |
| Keyword | Gingival | en |
| Keyword | Genetic Diseases | en |
| Keyword | Inborn | en |
| Publisher | Brieflands | en |
| Title | Hereditary gingival fibromatosis: a case report | en |
| Type | Case Report | en |