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Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management.
Pinna R, Cocco F, Campus G, Conti G, Milia E, Sardella A, Cagetti MG. Pinna R, et al. Periodontol 2000. 2019 Jun;80(1):12-27. doi: 10.1111/prd.12261. Periodontol 2000. 2019. PMID: 31090139 Review.
Other genetic disorders not included in the genodermatosis group and reported in the present review are: acanthosis nigricans, angio-osteo-hypertrophic syndrome, encephalotrigeminal angiomatosis, familial adenomatous polyposis, focal dermal hypoplasia, focal palmoplantar and oral …
Other genetic disorders not included in the genodermatosis group and reported in the present review are: acanthosis nigricans, angio-osteo-h …
Diagnosis and treatment of a hereditary gingival fibromatosis case.
Zhou M, Xu L, Meng HX. Zhou M, et al. Chin J Dent Res. 2011;14(2):155-8. Chin J Dent Res. 2011. PMID: 22319759 Free article.
Hereditary gingival fibromatosis (HGF) is a rare condition characterised by severe gingival hyperplasia, which could result in serious aesthetic and emotional problems and functional impairment. Here the present authors report a case of a 28-year-old female p …
Hereditary gingival fibromatosis (HGF) is a rare condition characterised by severe gingival hyperplasia, which could re …
Towards the targeted management of hereditary gingival fibromatosis.
Yussif NM, Abdul Aziz MA. Yussif NM, et al. Med Hypotheses. 2018 Dec;121:188-190. doi: 10.1016/j.mehy.2018.09.017. Epub 2018 Sep 10. Med Hypotheses. 2018. PMID: 30396478
Although hereditary gingival fibromatosis is a rare condition, it leaves unrestroable psychological, esthetical as well as functional problems to the affected patients. ...
Although hereditary gingival fibromatosis is a rare condition, it leaves unrestroable psychological, esthetical as well as fun …
Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Nitayavardhana I, Theerapanon T, Srichomthong C, Piwluang S, Wichadakul D, Porntaveetus T, Shotelersuk V. Nitayavardhana I, et al. Mol Genet Genomics. 2020 Jul;295(4):923-931. doi: 10.1007/s00438-020-01668-8. Epub 2020 Apr 3. Mol Genet Genomics. 2020. PMID: 32246227
A review of all 70 patients from 50 independent families with AI1G (including two families in this study) showed that the penetrance of hypoplastic enamel and gingival hyperplasia was complete. Unerupted permanent teeth were found in all 70 patients except Pt-2. ...A large …
A review of all 70 patients from 50 independent families with AI1G (including two families in this study) showed that the penetrance of hypo …