Literature DB >> 4061496

Gingival fibromatosis with sensorineural hearing loss: an autosomal dominant trait.

J K Hartsfield, D Bixler, R H Hazen.   

Abstract

Gingival fibromatosis is a heterogeneous entity that can occur both as a part of syndromes and as an isolated trait. We describe the second family with a rare, dominantly inherited syndrome of gingival fibromatosis and progressive sensorineural hearing loss.

Entities:  

Mesh：

Year:  1985        PMID： 4061496     DOI： 10.1002/ajmg.1320220323

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  6 in total

1.  Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21.

Authors:  T C Hart; D Pallos; D W Bowden; J Bolyard; M J Pettenati; J R Cortelli
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

2.  Gingival Fibromatosis with Distinctive Facies - A Three Generation Case Report.

Authors:  Sachin Kanagotagi; Sunil Sidana; Sneha Rajguru; Ashvini Padhye
Journal:  J Clin Diagn Res       Date:  2015-05-01

3.  Unusual clinical and histologic findings in a child with mixed dentition with hereditary gingival fibromatosis: a case report.

Authors:  Han Gao; Jun Liang; Xiaoxue Xia; Zhaoming Deng; Zhaoqiang Zhang
Journal:  Transl Pediatr       Date:  2020-02

4.  Rare Diseases with Periodontal Manifestations.

Authors:  Marcel Hanisch; Thomas Hoffmann; Lauren Bohner; Lale Hanisch; Korbinian Benz; Johannes Kleinheinz; Jochen Jackowski
Journal:  Int J Environ Res Public Health       Date:  2019-03-09       Impact factor: 3.390

Review 5.  Clinics and genetic background of hereditary gingival fibromatosis.

Authors:  Karolina Strzelec; Agata Dziedzic; Katarzyna Łazarz-Bartyzel; Aleksander M Grabiec; Ewa Gutmajster; Tomasz Kaczmarzyk; Paweł Plakwicz; Katarzyna Gawron
Journal:  Orphanet J Rare Dis       Date:  2021-11-24       Impact factor: 4.123

Review 6.  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
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.