Results 61 to 70 of about 1,146 (168)
Unusual Gingival Enlargement: A Rare Case Report
Case Reports in Dentistry, 2014 This is an atypical case report of a 20-year-old male patient who suffered from unusual unilateral, gingival enlargement together with rapidly progressive alveolar bone loss. The enlarged gingiva completely covered his left posterior teeth in both arches.
Ashutosh Dixit +2 more
doaj +1 more source
Idiopathic gingival fibromatosis with asymmetrical presentation and electrosurgical management
Journal of Indian Society of Periodontology, 2016 Idiopathic gingival fibromatosis is a rare genetically heterogeneous condition characterized by recurrent gingival enlargement without any identifiable cause.
Dilip Ganpat Pol +2 more
doaj +1 more source
Clinical Genetics, Volume 106, Issue 2, Page 199-203, August 2024.RASopathies, caused by variants in Ras/MAPK pathways, include newly associated MAP4K4 gene disorders. This study details a Korean boy with a de novo MAP4K4 variant, presenting craniofacial dysmorphism, developmental delays, and syndromic craniosynostosis, expanding the known phenotypic spectrum and underscoring MAP4K4's impact on cranial suture ...
Jihoon G. Yoon +4 more
wiley +1 more source
Case Reports in Dentistry, 2012 Amelogenesis imperfecta (AI) is a group of hereditary disorders primarily characterized by developmental abnormalities in the quantity and/or quality of enamel.
Emre Yaprak +3 more
doaj +1 more source
Contemporary Clinical Dentistry, 2012 Hereditary gingival fibromatosis is a rare condition characterized by various degree of gingival overgrowth. It usually develops as an isolated disorder but can manifest with multisystem syndrome.
Lata Goyal +3 more
doaj +1 more source
Clinical and Experimental Dental Research, Volume 10, Issue 3, June 2024.ABSTRACT Objectives Gingiva is one of the supporting tissues around the teeth that can be affected by various neoplastic or nonneoplastic lesions. Previous studies have examined several types of gingival lesions, but the lack of a standardized classification system has hindered meaningful comparisons.
Nafiseh Shamloo +2 more
wiley +1 more source
Hereditary Nonsyndromic Gingival Fibromatosis: Report of Family Case Series
Case Reports in Dentistry, 2013 Hereditary gingival fibromatosis (HGF) is a rare, benign disorder with slowly progressive enlargement of maxillary and mandibular gingiva. Herewith, we report the first case series of HGF presenting among mother and all of her 3 children.
Syed Wali Peeran +4 more
doaj +1 more source
Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome
Indian Journal of Dental Research, 2017 Gingival fibromatosis with hypertrichosis syndrome is an extremely rare genetic condition characterized by profound overgrowth of hair and gums, as well as other variable features.
Preetha Balaji, S M Balaji
doaj +1 more source
Zimmermann-Laband Syndrome: Report of a Case with Early Cardiac Complications
Journal of Indian Academy of Oral Medicine and Radiology, 2010 Laband syndrome (LS) is a rare autosomal dominant inherited disorder characterized by coarse facial appearance, gingival fibromatosis, and hypoplasia of the terminal phalanges and nails of hands and feet.
Atul P Sattur +3 more
doaj
HEREDITARY GINGIVAL FIBROMATOSIS
The Professional Medical Journal, 2018 Hereditary gingival fibromatosis also referred to as idiopathic gingival hyperplasia,elephantiasis gingivae etc; is a rare hereditary localized or generalized condition, whichrepresents as swelling of gingivae of varied degrees with no apparent cause.
Faheem Ahmed Pirwani +3 more
openaire +2 more sources