Literature DB >> 6652936

Perilymphatic gusher and stapes surgery. A predictable complication?

C W Cremers, G C Hombergen, R T Wentges.   

Abstract

The cases of 3 patients who had 'perilymph gushers' following stapes surgery are reported. The similarities in their clinical histories and examinations are discussed. All 3 were males and had progressive mixed deafness presenting in early childhood. Polytomography revealed anomalies in both the vestibule and internal auditory meatus in 1 patient; the stapedial reflex was unexpectedly large in all 3. Further preoperative evaluation of these features in other patients and patients affected by the X-linked deafness syndrome is indicated in order to assess the validity of the above criteria.

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Year:  1983        PMID: 6652936     DOI: 10.1111/j.1365-2273.1983.tb01434.x

Source DB:  PubMed          Journal:  Clin Otolaryngol Allied Sci        ISSN: 0307-7772


  4 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.  Molecular and clinical studies of X-linked deafness among Pakistani families.

Authors:  Ali M Waryah; Zubair M Ahmed; Munir A Bhinder; Munir A Binder; Daniel I Choo; Robert A Sisk; Mohsin Shahzad; Shaheen N Khan; Thomas B Friedman; Sheikh Riazuddin; Saima Riazuddin
Journal:  J Hum Genet       Date:  2011-06-02       Impact factor: 3.172

3.  Pou3f4-mediated regulation of ephrin-b2 controls temporal bone development in the mouse.

Authors:  Steven Raft; Thomas M Coate; Matthew W Kelley; E Bryan Crenshaw; Doris K Wu
Journal:  PLoS One       Date:  2014-10-09       Impact factor: 3.240

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

  4 in total

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