Disease | Features | Inheritance | Chromosomal region/gene locus |
---|---|---|---|
Gingivitis | The inflammatory response to a local irritant can lead to chronic hyperplastic gingivitis. Gingival enlargement is usually limited to areas affected by the irritant | Â | Â |
Drug-induced gingival overgrowth [21] | Intake of anticonvulsants, immunosuppressants, calcium channel blockers, or other drugs implicated in the occurrence of gingival overgrowth | Â | Â |
Gingival overgrowth associated with systemic diseases | |||
Leukemia [22] | Anemia, neutropenia, thrombocytopenia, easy fatigability, fever, bone pain, spontaneous gingival bleeding, gingival enlargement, petechial hemorrhages, mucosal pallor, herpetic infections, candidiasis, and oral ulceration | Â | Â |
Vitamin C deficiency [23] | Vitamin C deficiency is defined as a serum ascorbic acid level < 2 μg/mL. Clinical manifestations of scurvy include anemia, myalgia, bone pain, swelling, gingival enlargement, poor wound healing, and spontaneous bleeding |  |  |
Crohn’s disease [24] | Crohn’s disease is a chronic gastrointestinal inflammatory disease. Clinical manifestations include abdominal pain, diarrhea, nausea, vomiting, and weight loss. Oral manifestations include mucosal tags; swelling of the lips, cheeks, and gingiva; and cobblestone appearance of the mucosa |  |  |
Genetic diseases and syndromes | |||
Neurofibromatosis, type I (MIM 162200) [25] | Café-au-lait macules, axillary and inguinal freckling, neurofibromas, plexiform neurofibroma, optic pathway gliomas, sphenoid wing dysplasia or long-bone dysplasia, and Lisch nodules | Autosomal dominant | 17q11.2 |
Hereditary gingival fibromatosis (MIM 135300, 605544, 609955 et al.) [26,27,28] | Benign, slow-growing, non-hemorrhagic, fibrous hyperplasia of the maxillary and mandibular gingiva | Autosomal dominant | 2p22.1, 5q13-q22, 2p23.3-p22.3 et al |
Congenital generalized hypertrichosis with or without gingival hyperplasia (MIM 135400) [29, 30] | Hypertrichosis, gingival hyperplasia, dysmorphic and coarse facies | Autosomal dominant, autosomal recessive | 17q24.2-q24.3 |
Mucolipidosis (MIM 252500, 252600) [31] | Short stature, skeletal abnormalities, cardiomegaly, developmental delay, and gingival hyperplasia | Autosomal recessive | 12q23.2 |
Winchester syndrome (MIM 277950) [32] | Generalized osteoporosis, multicentric osteolysis, and progressive joint destruction | Autosomal recessive | 14q11.2 |
Zimmermann-Laband syndrome (MIM 135500, 616455, 618658) [33,34,35] | Gingival fibromatosis, hypo/aplastic nails and distal phalanges, hepatosplenomegaly, hypertrichosis, joint hypermobility, and abnormalities of the cartilage of the nose and/or ears | Autosomal dominant | 1q32.2, 8p21.3, 1q21.3 |
Frank-ter Haar syndrome (MIM 249420) [36] | Thick skin, osteolysis, gingival hypertrophy, craniofacial anomalies, skeletal dysplasia, and cardiac defects | Autosomal recessive | 5q35.1 |
Amelogenesis imperfecta, type IG (MIM 204690) [37] | Generalized thin hypoplastic or absent enamel in the primary and permanent teeth, pulp stones, delayed tooth eruption, root dilacerations of impacted teeth, gingival hyperplasia, and nephrocalcinosis | Autosomal recessive | 17q24.2 |
Raine syndrome (MIM 259775) [38] | Generalized osteosclerosis, craniofacial dysplasia, thoracic hypoplasia, and gingival hyperplasia | Autosomal recessive | 7p22.3 |
Gingival fibromatosis with progressive deafness (MIM 135550) [39] | Gingival fibromatosis associated with progressive neural hearing loss | Autosomal dominant | / |
Gingival fibromatosis with distinctive facies (MIM 228560) [40] | Gingival fibromatosis, macrocephaly, bushy eyebrows, synophrys, hypertelorism, downslanting palpebral fissures, flattened nasal bridge, hypoplastic nares, cupid-bow mouth, and highly arched palate | Autosomal recessive | / |
Gingival fibromatosis, cherubism, short stature, mental deficiency, hypertrichosis, juvenile rheumatoid arthritis, and epilepsy | Autosomal recessive | / | |
Failure of eruption of teeth, gingival hyperplasia, dense corneal opacities | Autosomal dominant | / |