Immunoexpression of α2-integrin and Hsp47 in hereditary gingival fibromatosis and gingival fibromatosis-associated dental abnormalities. [PDF]
Med Oral Patol Oral Cir Bucal, 2013 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Objective: The purpose of the present study was to investigate the expression of the alpha 2-integrin subunit and heat shock protein 47 (Hsp47) in two families with isolated gingival ...
Vieira-Júnior JR +5 more
europepmc +5 more sources
Diode laser versus scalpel in the treatment of hereditary gingival fibromatosis in a 6-year old boy [PDF]
Clinics and Practice, 2016 Hereditary gingival fibromatosis (HGF) is a rare disease characterized by a benign enlargement of the gingiva involving both the mandible and the maxilla.
Samia Aboujaoude +2 more
doaj +2 more sources
Hereditary gingival fibromatosis: A report of two cases in the same family
Journal of International Clinical Dental Research Organization, 2016 Overgrowth of keratinized gingival tissues is a common condition and is described under variety of names. Causes of such enlargement can be medications, hereditary, and/or local irritating factors.
Vanali V Umrania +3 more
doaj +2 more sources
Zimmermann-Laband-1 Syndrome: Clinical, Histological, and Proteomic Findings of a 3-Year-Old Patient with Hereditary Gingival Fibromatosis [PDF]
Biomedicines, 2019 Background: Zimmermann-Laband-1 syndrome (ZLS-1; OMIM# 135500) is a rare genetic disorder whose oral pathognomonic sign is the development of progressive, diffuse, and severe gingival hypertrophy.
Federica Guglielmi +4 more
doaj +2 more sources
Hereditary Gingival Fibromatosis: A Report of a Severe Case. [PDF]
Cureus, 2022 Hereditary gingival fibromatosis (HGF) is an uncommon condition characterized by a benign, local, or diffuse gingival overgrowth. It may cover the teeth partially or totally, causing essential aesthetic, phonetic, and masticatory disorders. In this report, we discuss a case of an 11-year-old boy who presented with severe gingival enlargement.
Aboujaoude S, Aoun G.
europepmc +3 more sources
Ultrastructural Evaluation Of Gingival Connective Tissue In Hereditary Gingival Fibromatosis
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2016 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)To describe the ultrastructural features of hereditary gingival fibromatosis (HGF) in affected family members and compare microscopic findings with normal gingival (NG) tissue.
RD; de Aquino +6 more
core +3 more sources
Familial gingival fibromatosis: A rare case report
Contemporary Clinical Dentistry, 2012 Hereditary gingival fibromatosis is a rare condition that can occur as an isolated disease or as part of a syndrome or chromosomal abnormality. In severe cases, the gingival enlargement may cover the crowns of teeth and cause severe functional and ...
Shweta Sharma +3 more
doaj +2 more sources
Hereditary gingival fibromatosis. [PDF]
Natl J Maxillofac Surg, 2014 Hereditary gingival fibromatosis (HGF) is a rare condition that can occur as an isolated disease, chromosomal abnormality, or as part of a number of syndromes. The gingival enlargement in HGF can be so severe that it can cover the crowns of teeth completely, causing severe functional derangement and facial disfigurement.
Chaurasia A.
europepmc +4 more sources
Hereditary gingival fibromatosis. [PDF]
J Indian Soc Periodontol, 2012 Hereditary gingival fibromatosis is a rare benign oral condition characterised by slow and progressive enlargement of both maxillary and mandibular attached gingiva. It may develop as an isolated disorder but can feature along with a syndrome. A case of 12 year old female child who presented with generalised severe gingival overgrowth, involving both ...
Dhadse PV +3 more
europepmc +3 more sources
Analysis of Mutations in the SOS-1 Gene in Two Polish Families With Hereditary Gingival Fibromatosis [PDF]
Oral Diseases, 2017 Renata Górska +2 more
exaly +2 more sources