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Abstract

Hereditary gingival fibromatosis is a rare genetic dis order that may exist as an isolated disease entity or as part of a syndrome.

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  • Aldred MI, Bartold PM (2000) Genetic disorders of the gingivac and periodontium. Periodontol 2000 18:7–20

    Article  Google Scholar 

  • Apaydin A (1995) Ehlers-Danlos syndrome (type VIII). J Nihon Univ Sch Dent 37:214–217

    Article  PubMed  Google Scholar 

  • Austin GB, Quart AM, Novak B (1981) Hereditary hemorrhagic telangiectasia with oral manifestations. Oral Surg Oral Med Oral Pathol 51:245–251

    Article  PubMed  Google Scholar 

  • Baab DA, Page RC, Ebersoie IL, et al (1986) Laboratory studies of a family manifesting premature exfoliation of deciduous teeth. J Clin Periodontol 13:677–683

    Article  PubMed  Google Scholar 

  • Bakaeen G, Scully C (1991) Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome. J Oral Pathol Med 20:457–459

    Article  PubMed  Google Scholar 

  • Barabas GM (1969) Ehlers-Danlos syndrome. Abnormalities of the enamel, dentine, cementum and the dental pulp: a histologic examination of 24 teeth from 6 patients. Br Dent J 126:509–515

    PubMed  Google Scholar 

  • Barrett AP, Buckley DI, Katelaris CH (1990) Oral complications in type Ib glycogen storage disease. Oral Surg Oral Med Oral Pathol 69:174–176

    Article  PubMed  Google Scholar 

  • Bazopoulou-Kyrkanidou E, Papagianoulis L, Papanicolaou S, Mavrou A (1990) Laband syndrome: a case report. J Oral Pathol Med 19:385–387

    Article  PubMed  Google Scholar 

  • Bazopoulou E, Laskaris G, Katsabas A, Papanikolaou S (1991) Familial benign acanthosis nigricans with predominant early oral manifestations. Clin Genet 40:160

    Google Scholar 

  • Beumer I, Trowbridge HO, Silverman S Jr, Eisenberg E (1973) Childhood hypophosphatasia and the premature loss of teeth: a clinical and laboratory study of seven cases. Oral Surg Oral Med Oral Pathol 35:631–640

    Article  PubMed  Google Scholar 

  • Bozzo L, Almeida O, Scully C, Aldred MI (1994) Hereditary gingival fibromatosis. Oral Surg Oral Med Oral Pathol 78:452–454

    Article  PubMed  Google Scholar 

  • Breton P, Cambazard M, Rougier M, et al (1988) Manifestations maxillofaciales de la maladie de Cowden. Apropos de deux observations. Rev Stomatol Chir Maxillofac 89:87–91

    PubMed  Google Scholar 

  • Camisa C, Bikowski JB, McDonald SG (1984) Cowden’s disease: association with squamous cell carcinoma of the tongue and perianal basal cell carcinoma. Arch Dermatol 120:677–678

    Article  PubMed  Google Scholar 

  • Charon JA, Mergenhagen SE, Gallin JI (1985) Gingivitis and oral ulceration in patients with neutrophil dysfunction. J Oral Pathol 14:150–155

    Article  PubMed  Google Scholar 

  • Ellis RWB, Andrew JD (1962) Chondroectodermal dysplasia. J Bone Surg 44B:626–636

    Google Scholar 

  • Everett FG, Hahn CR (1976) Hereditary hemorrhagic telangiectasia with gingival lesions: review and case reports. J Periodontol 47:295–298

    PubMed  Google Scholar 

  • Fenerly A, Laskaris G (1984) Oral manifestation of Darier’s disease. Hell Stomatol Rev 28:40–46

    Google Scholar 

  • Ferris T, Lamey PJ, Rennie JS (1990) Darier’s disease: oral features and genetic aspects. Br Dent J 168:71–73

    Article  PubMed  Google Scholar 

  • Flint SR, Keith O, Scully C (1988) Hereditary hemorrhagic telangiectasia: family study and review. Oral Surg Oral Med Oral Pathol 66:440–444

    Article  PubMed  Google Scholar 

  • Gardner DG (1971) The oral manifestations of Hurler’s syndrome. Oral Surg Oral Med Oral Pathol 32:46–57

    Article  PubMed  Google Scholar 

  • Goltz EW, Henderson RR, Hitch JM, Ott JE (1970) Focal dermal hypoplasia syndrome: a review of the literature review. Arch Dermatol 101:1–11

    Article  PubMed  Google Scholar 

  • Gomez MR (1988) Tuberous sclerosis. Raven Press, New York

    Google Scholar 

  • Gorlin RT, Cohen MM, Levin LS (1990) Syndromes of the head and neck. Oxford University Press, New York

    Google Scholar 

  • Hall EH, Terezhalmy GT (1983) Focal dermal hypoplasia syndrome: case report and literature review. J Am Acad Dermatol 9:443–451

    Article  PubMed  Google Scholar 

  • Hamilton RE, Giamsanti JS (1974) Chédiak-Higashi syndrome: report of a case and review of the literature. Oral Surg Oral Med Oral Pathol 37:754–761

    Article  PubMed  Google Scholar 

  • Hanake E (1979) The Papillon-Lefevre syndrome: keratosis palmoplantaris with periodontopathy. Report of a case and review of the cases in the literature. Hum Genetics 51:1–35

    Article  Google Scholar 

  • Hara T, Mizumo Y, Okubo K, Veda K (1987) Glycogenesis type Ib and periodontitis. J Pediatr 111:952

    PubMed  Google Scholar 

  • Harned RK, Buck JL, Olmsted WW et al (1991) Extracolonic manifestations of the familial adenomatous polyposis syndromes. Am J Roentgenol 156:481–485

    Google Scholar 

  • Hartsfield JK, Kousseff BG (1990) Phenotype overlap of Ehlers-Danlos syndrome types IV and VIII. Am J Med Genet 37:465–470

    Article  PubMed  Google Scholar 

  • Hochberg MS, Vazquez-Santiago IA, Sher M (1993) Epidermolysis bullosa. Oral Surg Oral Med Oral Pathol 75:54–57

    Article  PubMed  Google Scholar 

  • Hopwood JJ, Morris CP (1990) The mucopolysaccharidoses: diagnosis, molecular genetics and treatment. Mol Biol Med 7:381–404

    PubMed  Google Scholar 

  • Kinane D (1999) Blood and lymphoreticular disorders. Periodontol 2000 21:84–93

    Article  PubMed  Google Scholar 

  • Kinane D (1999) Periodontitis modified by systemic factors. Ann Periodontol 4:54–63

    Article  PubMed  Google Scholar 

  • Krajewska IA, Moore L, Brown JH (1992) White sponge nevus presenting in the esophagus: case report and literature review. Pathology 24:112–115

    Article  PubMed  Google Scholar 

  • Laskaris G, Vareltzidis A, Avgerinou G (1980) Focal palmoplantar and oral mucosa hyperkeratosis syndrome: areport concerning five members of a family. Oral Surg Oral Med Oral Pathol 50:250–253

    Article  PubMed  Google Scholar 

  • Laskaris G (2000) Color atlas of oral diseases in children and adolescents. Georg Thieme Verlag, Stuttgart

    Google Scholar 

  • Lipp MJ, Lubit EC (1990) The oral-facial-digital syndrome: case report of a mother and daughter. Cleft Palate 27:311–316

    Google Scholar 

  • Lygidakis NA, Lindnebaum RH (1989) Oral fibromas in tuberous sclerosis. Oral Surg Oral Med Oral Pathol 68:725–728

    Article  PubMed  Google Scholar 

  • Mackler SB, Shoulars HW, Burker EJ (1972) Tuberous sclerosis with gingivallesions. Oral Surg Oral Med Oral Pathol 34:619–624

    Article  PubMed  Google Scholar 

  • Orner G (1976) Periodontal disease among children with Down’s syndrome and their siblings. J Dent Res 55:778–782

    Article  PubMed  Google Scholar 

  • Page RC, Beck JD (1997) Risk assessment for periodontal diseases. Int Dent J 47:61–87

    Article  PubMed  Google Scholar 

  • Pindborg JJ, Gorlin RJ (1962) Oral changes in acanthosis nigricans: juvenile type. Acta Derm Venereol (Stockh) 42:63–71

    Google Scholar 

  • Salapata J, Laskaris G, Drogari E et al (1995) Oral manifestations in glycogen storage disease type Ib. J Oral Pathol Med 24:136–139

    Article  PubMed  Google Scholar 

  • Salinas CF, Pai GS, Vera CL et al (1991) Variability of expression of the orofacial digital syndrome type I in black females: six cases. Am J Med Genet 38:574–582

    Article  PubMed  Google Scholar 

  • Saxén L, Aula S (1982) Periodontal bone loss in patients with Down’s syndrome: a follow-up study. J Periodontol 53:158–162

    Article  PubMed  Google Scholar 

  • Sciubba JJ, Brown AM (1977) Oral-facial manifestations of Klippel-Trenaunay-Weber syndrome. Oral Surg Oral Med Oral Pathol 43:227–232

    Article  PubMed  Google Scholar 

  • Smith DB, Strand JA, Carter PL (1988) Gardner’s syndrome: current concepts and use of a new genetic marker. Mil Med 153:289–293

    PubMed  Google Scholar 

  • Steiner M, Could AR, Graves SM, Kuerschner TW (1987) Klippel-Trenaunay-Weber syndrome. Oral Surg Oral Med Oral Pathol 63:208–215

    Article  PubMed  Google Scholar 

  • Stewart RE, Hollister DW, Rimoin DL ( A new variant of Ehlers-Danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring and generalized periodontitis. Birth Defects 13:85–93

    Google Scholar 

  • Swart JG, Lekkas C, Allard RHB (1985) Oral manifestations in Cowden’s syndrome. Oral Surg Oral Med Oral Pathol 59:264–268

    Article  PubMed  Google Scholar 

  • Tasjian D, Jarrat M (1984) Familial acanthosis nigricans. Arch Dermatol 120:1351–1354

    Article  PubMed  Google Scholar 

  • Temple TR, Kimball HR, Kakehashi S, Amen CR (1972) Host factors in periodontal disease: periodontal manifestations of Chediak-Higashi syndrome. J Periodont Res 10 [Suppl]:26–27

    Google Scholar 

  • Tumber-Saini SK, Habbick BF, Oles AM et al (1992) The role of saliva in aggregation and adherence of Pseudomonas aeruginosa in patients with cystic fibrosis. J Oral Pathol Med 21:299–304

    Article  PubMed  Google Scholar 

  • Uitto J, Christiano AM (1993) Inherited epidermolysis bullosa: clinical features, molecular genetics, and pathoetiologic mechanisms. Dermatol Clin 11:549–563

    PubMed  Google Scholar 

  • Vasilopoulou A, Laskaris G (1989) Papillon-Lefevre syndrome: report of two brothers. J Dent Child, September-October:388–391

    Google Scholar 

  • Watanabe H, Umeda M, Seki T, Ishikawa I (1993) Clinical and laboratory studies of severe periodontal disease in an adolescent associated with hypophosphatasia: a case report. J Periodontol 64:174–180

    Article  PubMed  Google Scholar 

  • Winter GB, Geddes M (1967) Oral manifestations of chondroectodermal dysplasia (Ellis-van Creveld syndrome). Br Dent J 122:103–107

    PubMed  Google Scholar 

  • Wright JT (1991) Oral soft tissues in hereditary epidermolysis bullosa. Oral Surg Oral Med Oral Pathol 71:440–446

    Article  PubMed  Google Scholar 

  • Zachariades N (1987) Gardner’s syndrome: report of a family. J Oral Maxillofac Surg 45:438–440

    Article  PubMed  Google Scholar 

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Laskaris, G., Scully, C. (2003). Genetic Disorders. In: Periodontal Manifestations of Local and Systemic Diseases. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-55596-1_16

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  • DOI: https://doi.org/10.1007/978-3-642-55596-1_16

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-62788-0

  • Online ISBN: 978-3-642-55596-1

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