Outline
Hereditary gingival fibromatosis: a case report
Authors
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.
Case report: A 16 year old girl with esthetic problem referred to shahid beheshti medical sciences university, dental school. Based on medical history and clinical appearance of the patient, HGF was diagnosis. The patient treated with periodontal surgery and followed for six months. The result of treatment was successful after 6 months.
References
- 1.References are available in pdf.
Copyright
© 2013, Annals of Military and Health Sciences Research. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.
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