How to prevent a stapes gusher

Advances in Oto-Rhino-Laryngology

Volumn 65, Issue , 2007, Pages 278-284

  Cremers, C W R J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

POU3F4 PROTEIN, HUMAN; TRANSCRIPTION FACTOR POU; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ANAMNESIS; AUDITORY CANAL; CHILD; COMPUTER ASSISTED TOMOGRAPHY; CONDUCTION DEAFNESS; CONGENITAL MALFORMATION; FEMALE; FISTULA; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; HETEROZYGOTE DETECTION; HUMAN; INNER EAR DISEASE; MALE; MIXED HEARING LOSS; PEDIGREE; PERILYMPH; PEROPERATIVE COMPLICATION; PURE TONE AUDIOMETRY; RECESSIVE GENE; REVIEW; SEMICIRCULAR CANAL; SEX CHROMOSOME ABERRATION; STAPES SURGERY; SYNDROME; VESTIBULE; X CHROMOSOME;

ADOLESCENT; ADULT; AUDIOMETRY, PURE-TONE; CHILD; COCHLEAR DISEASES; EAR CANAL; FEMALE; FISTULA; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HEARING LOSS, CONDUCTIVE; HEARING LOSS, MIXED CONDUCTIVE-SENSORINEURAL; HETEROZYGOTE DETECTION; HUMANS; INTRAOPERATIVE COMPLICATIONS; MALE; MEDICAL HISTORY TAKING; PEDIGREE; PERILYMPH; POU DOMAIN FACTORS; SEMICIRCULAR CANALS; SEX CHROMOSOME ABERRATIONS; STAPES SURGERY; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED; VESTIBULE; X CHROMOSOME;

EID: 33846564935     PISSN: 00653071     EISSN: None     Source Type: Book Series    
DOI: 10.1159/000098843     Document Type: Review

References (17)

1. Glasscock ME: The stapes gusher. Arch Otolaryngol 1973;98:82-91.
2. Nance WE, Setleff R, McLeod A, Sweeney A, Cooper C, McConnell F: X-linked mixed deafness with congenital fixture of the stapedial footplate and perilymphatic gusher. Birth Defects Orig Artic Ser 1971;7:64-69.
3. Cremers CWRJ, Hombergen GCJH, Scaff JJ, Huygen PLM, Volkers WS, Pinckers AJLG: X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery. Arch Otolaryngol 1985;111:249-254.
4. Phelps PD, Reardon W, Pembrey M, Bellman S, Luxon L: X-linked deafness, stapes gushers and a distinctive defect of the inner ear. Neuroradiology 1991;33:326-330.
5. Michel O, Breunsbach J, Matthias R: Das angeborene Liquordrucklabyrinth. HNO 1991;39: 486-490.
6. Talbot JM, Wilson DF: Computed tomographic diagnosis of X-linked congenital mixed deafness, fixation of the stapedial footplate, and perilymphatic gusher. Am J Otol 1994;15:177-182.
7. Tang A, Parnes LS: X-linked progressive mixed hearing loss: computed tomography findings. Ann Otol Rhinol Laryngol 1994;103:655-657.
8. Cremers CWRJ: Audiological features of the X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes surgery. Am J Otol 1985;6:243-246.
9. Snik AFM, Hombergen GCJH, Mylanus EAM, Cremers CWRJ: Air-bone gap in patients with the X-linked stapes gusher syndrome. Am J Otol 1995;16:241-246.
10. Cremers CWRJ, Huygen PLM: Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery). Int J Pediatr Otolaryngol 1983;6:179-185.
11. Snik A, Mylanus E, Cremers CWRJ: Audiological characteristics of patients with X-linked stapes gusher syndrome; in Ernst A, Marchbanks R, Samii M (eds): Intracranial and Intralabyrinthine Fluids. Basic Aspects and Clinical Applications. Berlin, Springer, 1996, pp 239-243.
12. Cremers CWRJ, Hombergen GCJH, Wentges RTLR: Perilymphatic gusher and stapes surgery. A predictable complication? Clin Otolaryngol 1983;8:235-240.
13. De Kok YJM, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FPM: Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 1995;267:685-688.
14. De Kok YJM, Vossenaar ER, Cremers CWRJ, Dahl N, Laporte J, Hu LJ, Lacombe D, Fischel-Ghodsian N, Friedman RA, Parnes LS, Thorpe P, Bitner-Glindzicz M, Pander HJ, Heilbronner H, Gravelin J, den Dunnen JT, Brunner HG, Ropers HH, Cremers FPM: Identification of a hot spot for microdeletions in patients with X-linked deafness (DFN3) 900 kb proximal to the DFN3 gene POU3F4. Hum Mol Genet 1996;5:1229-1235.
15. De Kok YJM, Cremers CWRJ, Ropers HH, Cremers FPM: The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation. Hum Mutat 1997;10:207-211.
16. Cremers FPM, Cremers CWRJ, Ropers HH: The ins and outs of X-linked deafness type 3; in Kitamura K, Steel KP (eds): Genetics in Oto-Rhino- Laryngology. Basel, Karger, 2000, vol 56, pp 184-195.
17. Cremers CWRJ, Snik AFM, Huygen PLM, Joosten FBM, Cremers FPM: X-linked mixed deafness syndrome with congenital footplate fixation of the stapedial footplate and perilymphatic gusher (DFN3) Adv Otorhinolaryngol 2002;61:161-167.