Journal of International Clinical Dental Research Organization (Jan 2016)

Hereditary gingival fibromatosis: A report of two cases in the same family

  • Vanali V Umrania,
  • Nagarjuna VY Reddy,
  • Deepika Pawar Chandrashekhara Rao,
  • Usha Hegde

DOI
https://doi.org/10.4103/2231-0754.186423
Journal volume & issue
Vol. 8, no. 2
pp. 129 – 132

Abstract

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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. Mutation in SOS1, son-of-sevenless gene, is thought to be responsible for hereditary gingival fibromatosis. This report shows a case of 19-year-old male and his 15-year-old sister, with a chief complaint of overgrowth of gingival and irregularly placed teeth. A similar overgrowth was also found in other members of the same family, without any drug history or syndromic conditions. An occurrence of the disease has been found in two generations of this family and therefore, it may be following autosomal dominant trait of inheritance. Since it is idiopathic and has a genetic cause for its occurrence, it cannot be prevented. Both cases underwent a surgical intervention to rectify the abnormality and were followed from 6 months to 1 year, during which there was no recurrence.

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