Literature DB >> 4950923

Heterogeneity in gingival fibromatosis.

C J Witkop.   

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.

Entities:  

Mesh:

Year:  1971        PMID: 4950923

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  10 in total

1.  Characterization of fibroblasts with Son of Sevenless-1 mutation.

Authors:  E J Lee; S I Jang; D Pallos; J Kather; T C Hart
Journal:  J Dent Res       Date:  2006-11       Impact factor: 6.116

2.  Rare case report of idiopathic gingival fibromatosis in childhood and its management.

Authors:  Morankar Rahul; Krishan Gauba; Nitin Gorwade; Aman Kumar
Journal:  BMJ Case Rep       Date:  2019-01-22

3.  Gingival enlargement in acromegaly.

Authors:  I Capoglu; A B Yilmaz; N Unüvar; R Orbak; H Aksoy; H Yesilyurt
Journal:  Endocrine       Date:  2002-08       Impact factor: 3.633

4.  A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1.

Authors:  Thomas C Hart; Yingze Zhang; Michael C Gorry; P Suzanne Hart; Margaret Cooper; Mary L Marazita; Jared M Marks; Jose R Cortelli; Debora Pallos
Journal:  Am J Hum Genet       Date:  2002-02-26       Impact factor: 11.025

5.  An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis.

Authors:  A D Irvine; O M Dolan; D R Hadden; F J Stewart; E A Bingham; N C Nevin
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

Review 6.  Gingival enlargements: Differential diagnosis and review of literature.

Authors:  Amit Arvind Agrawal
Journal:  World J Clin Cases       Date:  2015-09-16       Impact factor: 1.337

7.  A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15.

Authors:  Yufei Zhu; Wenxia Zhang; Zhenghao Huo; Yi Zhang; Yu Xia; Bo Li; Xiangyin Kong; Landian Hu
Journal:  Hum Genet       Date:  2006-10-31       Impact factor: 4.132

8.  Multispeciality approach in the management of patient with hereditary gingival fibromatosis: 1-year followup: a case report.

Authors:  T Ramakrishnan; Manmeet Kaur
Journal:  Int J Dent       Date:  2010-12-23

9.  A novel gene ZNF862 causes hereditary gingival fibromatosis.

Authors:  Juan Wu; Dongna Chen; Hui Huang; Ning Luo; Huishuang Chen; Junjie Zhao; Yanyan Wang; Tian Zhao; Siyuan Huang; Yang Ren; Teng Zhai; Weibin Sun; Houxuan Li; Wei Li
Journal:  Elife       Date:  2022-02-10       Impact factor: 8.140

Review 10.  Gingival fibromatosis: clinical, molecular and therapeutic issues.

Authors:  Katarzyna Gawron; Katarzyna Łazarz-Bartyzel; Jan Potempa; Maria Chomyszyn-Gajewska
Journal:  Orphanet J Rare Dis       Date:  2016-01-27       Impact factor: 4.123

  10 in total

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