Literature DB >> 890092

Familial gingival fibromatosis associated with progressive deafness in five generations of a family.

G Jones, R S Wilroy, V McHaney.   

Abstract

Gingival hyperplasia may be inherited in a variety of ways, usually in an autosomal dominant or autosomal recessive manner. Additional phenotypic abnormalities are frequently associated with the gingival hyperplasia. To our knowledge, the family described here represents the first instance of autosomal dominantly inherited gingival hyperplasia associated with progressive neural hearing loss.

Entities:  

Mesh:

Year:  1977        PMID: 890092

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


  6 in total

1.  Imaging evalution of the gingival fibromatosis and dental abnormalities syndrome.

Authors:  Pe dos Santos Neto; Lan dos Santos; R D Coletta; A L Laranjeira; C C de Oliveira Santos; P R Bonan; H Martelli-Júnior
Journal:  Dentomaxillofac Radiol       Date:  2011-05       Impact factor: 2.419

2.  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

Review 3.  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 4.  Gingival fibromatosis with multiple unusual findings: report of a rare case.

Authors:  Long He; Fei-Yun Ping
Journal:  Int J Oral Sci       Date:  2012-09-07       Impact factor: 6.344

5.  Idiopathic gingival fibromatosis associated with progressive hearing loss: A nonfamilial variant of Jones syndrome.

Authors:  Bagavad Gita; Sajja Chandrasekaran; Prakash Manoharan; Garima Dembla
Journal:  Contemp Clin Dent       Date:  2014-04

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

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