Literature DB >> 6662621

Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery).

C W Cremers, P L Huygen.   

Abstract

A new pedigree with 9 obligate and 10 probable female carriers of the X-linked mixed deafness syndrome is presented. In the male the syndrome is characterized by a perilymphatic gusher during stapes surgery, a severe progressive mixed hearing loss and lack or strong reduction of vestibular responses. Four of the 9 obligate heterozygote females show similar but much milder audiological abnormalities. The other five obligate female carriers have a normal audiogram. None of the obligate female carriers showed vestibular abnormalities such as observed in the affected males. Ten females, sisters of affected males, have a chance of 50% to be heterozygote carriers. Five of these females have also a hearing loss, the other 5 have normal audiograms. The relevance of these findings for genetic counseling and for identification of affected males is discussed.

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Year:  1983        PMID: 6662621     DOI: 10.1016/s0165-5876(83)80118-9

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  5 in total

1.  X-linked deafness, stapes gushers and a distinctive defect of the inner ear.

Authors:  P D Phelps; W Reardon; M Pembrey; S Bellman; L Luxom
Journal:  Neuroradiology       Date:  1991       Impact factor: 2.804

2.  The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors:  H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

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.  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

5.  Revision Stapedectomy in a Female Patient with Inner Ear Malformation.

Authors:  Tirth R Patel; Aaron C Moberly
Journal:  Case Rep Otolaryngol       Date:  2016-04-06
  5 in total

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