Literature DB >> 9109724

Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher.

R A Friedman1, Y Bykhovskaya, G Tu, J M Talbot, D F Wilson, L S Parnes, N Fischel-Ghodsian.   

Abstract

The molecular defect in some patients with X-linked mixed deafness with perilymphatic gusher at stapes surgery (DFN3) was recently attributed to mutations in the POU3F4 gene. In this manuscript we describe the molecular analysis of the POU3F4 gene in 5 patients with clinical and radiographic evidence of DFN3. Novel mutations were found in 2 of the 5 patients analyzed, while 3 had an entirely normal protein coding sequence. The fact that 3 of the 5 patients with clinical histories and radiographic abnormalities characteristic of X-linked mixed deafness with perilymphatic gusher displayed normal POU3F4 gene sequences supports the possibility that not all patients with the characteristic phenotype have involvement of the POU3F4 gene.

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Year:  1997        PMID: 9109724     DOI: 10.1177/000348949710600411

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  8 in total

1.  Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.

Authors:  Abram P Vore; Eugene H Chang; Jane E Hoppe; Merlin G Butler; Shawnia Forrester; Michael C Schneider; Luke L H Smith; Daniel W Burke; Colleen A Campbell; Richard J H Smith
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2005-12

2.  De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.

Authors:  Hideaki Moteki; A Eliot Shearer; Shuji Izumi; Yamato Kubota; Hela Azaiez; Kevin T Booth; Christina M Sloan; Diana L Kolbe; Richard J H Smith; Shin-Ichi Usami
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-03-19       Impact factor: 1.547

3.  X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.

Authors:  Gregory J Anger; Susan Crocker; Kyle McKenzie; Kerry K Brown; Cynthia C Morton; Karen Harrison; Jennifer J MacKenzie
Journal:  Am J Audiol       Date:  2014-03       Impact factor: 1.493

4.  A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.

Authors:  Ahmet M Tekin; Marco Matulic; Wim Wuyts; Masoud Zoka Assadi; Griet Mertens; Vincent van Rompaey; Yongxin Li; Paul van de Heyning; Vedat Topsakal
Journal:  Genes (Basel)       Date:  2021-04-21       Impact factor: 4.096

5.  A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Authors:  Wan Du; Ming-Kun Han; Da-Yong Wang; Bing Han; Liang Zong; Lan Lan; Ju Yang; Qi Shen; Lin-Yi Xie; Lan Yu; Jing Guan; Qiu-Ju Wang
Journal:  Chin Med J (Engl)       Date:  2017-01-05       Impact factor: 2.628

6.  Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.

Authors:  Yu Su; Xue Gao; Sha-Sha Huang; Jing-Ning Mao; Bang-Qing Huang; Jian-Dong Zhao; Dong-Yang Kang; Xin Zhang; Pu Dai
Journal:  BMC Med Genet       Date:  2018-09-04       Impact factor: 2.103

7.  Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.

Authors:  Agnieszka Pollak; Urszula Lechowicz; Anna Kędra; Piotr Stawiński; Małgorzata Rydzanicz; Mariusz Furmanek; Małgorzata Brzozowska; Maciej Mrówka; Henryk Skarżyński; Piotr H Skarżyński; Monika Ołdak; Rafał Płoski
Journal:  PLoS One       Date:  2016-12-12       Impact factor: 3.240

8.  A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.

Authors:  Bang-Qing Huang; Jia-Ling Zeng; Yong-Yi Yuan; Pu Dai
Journal:  J Otol       Date:  2015-09-30
  8 in total

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