Literature DB >> 5173351

X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher.

W E Nance, R Setleff, A McLeod, A Sweeney, C Cooper, F McConnell.   

Abstract

An X-linked syndrome characterized in males by profound mixed deafness, vestibular abnormalities, congenital fixation of the stapes and perilymphatic otorrhea on attempted stapedectomy has been documented in a large Caucasian kindred. Female heterozygotes have similar but milder audiologic abnormalities. The syndrome of congenital fixation of the stapes with perilymphatic gusher may be a relatively common form of X-linked deafness and is an important clinical entity because affected males may be significantly benefited by sound amplification.

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Year:  1971        PMID: 5173351

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


  28 in total

1.  Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Authors:  I Bach; D Robinson; N Thomas; H H Ropers; F P Cremers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).

Authors:  I Bach; H G Brunner; P Beighton; R H Ruvalcaba; W Reardon; M E Pembrey; S D van der Velde-Visser; G A Bruns; C W Cremers; F P Cremers
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

Review 3.  Conductive hearing loss caused by third-window lesions of the inner ear.

Authors:  Saumil N Merchant; John J Rosowski
Journal:  Otol Neurotol       Date:  2008-04       Impact factor: 2.311

4.  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

5.  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

6.  Congenital stapesankylosis and fusion of tarsal and carpal bones as a dominant hereditary syndrome.

Authors:  H Spoendlin
Journal:  Arch Otorhinolaryngol       Date:  1974

7.  [Incomplete partition type III revisited-long-term results following cochlear implant. German version].

Authors:  A Alballaa; A Aschendorff; S Arndt; T Hildenbrand; C Becker; F Hassepass; R Laszig; R Beck; I Speck; T Wesarg; M C Ketterer
Journal:  HNO       Date:  2019-10       Impact factor: 1.284

8.  A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations.

Authors:  J-A Prat Matifoll; M Wilson; R Goetti; C Birman; B Bennett; E Peadon; A Prats-Uribe; K Prelog
Journal:  AJNR Am J Neuroradiol       Date:  2020-05-14       Impact factor: 3.825

9.  1992 American Society of Human Genetics presidential address: back to the future.

Authors:  W E Nance
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

Review 10.  New Imaging Findings of Incomplete Partition Type III Inner Ear Malformation and Literature Review.

Authors:  R Hong; Q Du; Y Pan
Journal:  AJNR Am J Neuroradiol       Date:  2020-05-28       Impact factor: 3.825

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