Heterogeneity in gingival fibromatosis

Birth Defects Orig Artic Ser. 1971 Jun;7(7):210-21.

Abstract

A review of cases indicated that gingival fibromatosis occurs in a variety of genetic entities. High risk for epilepsy and oligophrenia is associated if hypertrichosis is present. Other entities are symmetrical gingival fibromatosis; Zimmermann-Laband syndrome with bone, ear, nose and nail defects and hepatosplenomegaly; Murray syndrome with multiple hyaline dermal tumors; Rutherfurd syndrome with corneal dystrophy; Cowden syndrome with hypertrichosis, oligophrenia and giant fibroadenomatosis of breasts and Cross syndrome of hypopigmentation, oligophrenia and athetosis.

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / complications
  • Adenofibroma / complications
  • Albinism / complications
  • Anodontia / genetics
  • Athetosis / complications
  • Bone and Bones / abnormalities
  • Breast Neoplasms / complications
  • Corneal Dystrophies, Hereditary / genetics
  • Ear, External / abnormalities
  • Epilepsy / complications
  • Female
  • Fibroma / complications
  • Fibromatosis, Gingival / classification
  • Fibromatosis, Gingival / genetics*
  • Gingival Hypertrophy / genetics
  • Hepatomegaly / complications
  • Humans
  • Hypertrichosis / complications
  • Intellectual Disability / complications
  • Jaw Abnormalities / complications
  • Male
  • Microphthalmos / complications
  • Nails, Malformed / complications
  • Nose Deformities, Acquired
  • Splenomegaly / complications