Audiological profile of children and young adults with syndromic and complex craniosynostosis

Archives of Otolaryngology - Head and Neck Surgery

Volumn 137, Issue 8, 2011, Pages 775-778

  De Jong, Tim ^a   Toll, Martijn S ^a   De Gier, Henriëtte H W ^a   Mathijssen, Irene M J ^a  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ADOLESCENT; ADULT; ARTICLE; AUDIOMETRY; AUDITORY SYSTEM EXAMINATION; CHILD; COMPLEX CRANIOSYNOSTOSIS; CONDUCTION DEAFNESS; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; DISEASE SEVERITY; FEMALE; FOLLOW UP; HEARING LOSS; HUMAN; MAJOR CLINICAL STUDY; MALE; MUENKE SYNDROME; OUTCOME ASSESSMENT; PERCEPTION DEAFNESS; PRESCHOOL CHILD; SCHOOL CHILD; SECRETORY OTITIS MEDIA;

ACROCEPHALOSYNDACTYLIA; ADOLESCENT; AUDIOMETRY, PURE-TONE; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL DYSOSTOSIS; CRANIOSYNOSTOSES; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MENKES KINKY HAIR SYNDROME; OTITIS MEDIA; OTITIS MEDIA WITH EFFUSION;

EID: 84860410717     PISSN: 08864470     EISSN: 1538361X     Source Type: Journal    
DOI: 10.1001/archoto.2011.115     Document Type: Article

References (25)

1. De Jong T., Bannink N., Bredero-Boelhouwer H.H., et al. Long-term functional outcome in 167 patients with syndromic craniosynostosis: Defining a syndrome-specific risk profile. J Plast Reconstr Aesthet Surg. 2010;63(10):1635-1641.
2. Vallino-Napoli L.D. Audiologic and otologic characteristics of Pfeiffer syndrome. Cleft Palate Craniofac J. 1996;33(6):524-529. (Pubitemid 26392822)
3. Orvidas L.J., Fabry L.B., Diacova S., McDonald T.J. Hearing and otopathology in Crouzon syndrome. Laryngoscope. 1999;109(9):1372-1375. (Pubitemid 29426524)
4. Cremers C.W. Hearing loss in Pfeiffer's syndrome. Int J Pediatr Otorhinolaryngol. 1981;3(4):343-353. (Pubitemid 12178320)
5. Ensink R.J., Marres H.A., Brunner H.G., Cremers C.W. Hearing loss in the Saethre-Chotzen syndrome. J Laryngol Otol. 1996;110(10):952-957. (Pubitemid 26355868)
6. Lee S., Seto M., Sie K., Cunningham M. A child with Saethre-Chotzen syndrome, sensorineural hearing loss, and a TWIST mutation. Cleft Palate Craniofac J. 2002;39(1):110-114. (Pubitemid 34053011)
7. Rajenderkumar D., Bamiou D.E., Sirimanna T. Audiological profile in Apert syndrome. Arch Dis Child. 2005;90(6):592-593. (Pubitemid 40780719)
8. Shipster C., Hearst D., Dockrell J.E., Kilby E., Hayward R. Speech and language skills and cognitive functioning in children with Apert syndrome: A pilot study. Int J Lang Commun Disord. 2002;37(3):325-343. (Pubitemid 34925484)
9. Bergstrom L., Neblett L.M., Hemenway W.G. Otologic manifestations of acrocephalosyndactyly. Arch Otolaryngol. 1972;96(2):117-123.
10. Gould H.J., Caldarelli D.D. Hearing and otopathology in Apert syndrome. Arch Otolaryngol. 1982;108(6):347-349. (Pubitemid 12080255)
11. Kress W., Schropp C., Lieb G., et al. Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: Functional differentiation from Muenke coronal synostosis syndrome. Eur J Hum Genet. 2006;14(1):39-48. (Pubitemid 43019082)
12. Corey J.P., Caldarelli D.D., Gould H.J. Otopathology in cranial facial dysostosis. Am J Otol. 1987;8(1):14-17. (Pubitemid 17037137)
13. Peterson-Falzone S.J., Pruzansky S., Parris P.J., Laffer J.L. Nasopharyngeal dysmorphology in the syndromes of Apert and Crouzon. Cleft Palate J. 1981;18(4):237-250. (Pubitemid 11022330)
14. Niemelä M., Uhari M., Lautala P., Huggare J. Association of recurrent acute otitis media with nasopharynx dimensions in children. J Laryngol Otol. 1994;108(4):299-302. (Pubitemid 24125763)
15. Abramson D.L., Janecka I.P., Mulliken J.B. Abnormalities of the cranial base in synostotic frontal plagiocephaly. J Craniofac Surg. 1996;7(6):426-428. (Pubitemid 26413460)
16. Gozal D., Kheirandish-Gozal L., Capdevila O.S., Dayyat E., Kheirandish E. Prevalence of recurrent otitis media in habitually snoring school-aged children. Sleep Med. 2008;9(5):549-554. (Pubitemid 351837475)
17. Flynn T., Möller C., Jönsson R., Lohmander A. The high prevalence of otitis media with effusion in children with cleft lip and palate as compared to children without clefts. Int J Pediatr Otorhinolaryngol. 2009;73(10):1441-1446.
18. Huang F., Sweet R., Tewfik T.L. Apert syndrome and hearing loss with ear anomalies: A case report and literature review. Int J Pediatr Otorhinolaryngol. 2004;68(4):495-501. (Pubitemid 38328622)
19. Rajenderkumar D., Bamiou D., Sirimanna T. Management of hearing loss in Apert syndrome. J Laryngol Otol. 2005;119(5):385-390. (Pubitemid 40769339)
20. Zhou G., Schwartz L.T., Gopen Q. Inner ear anomalies and conductive hearing loss in children with Apert syndrome: An overlooked otologic aspect. Otol Neurotol. 2009;30(2):184-189.
21. Mikulec A.A., McKenna M.J., Ramsey M.J., et al. Superior semicircular canal dehiscence presenting as conductive hearing loss without vertigo. Otol Neurotol. 2004;25(2):121-129. (Pubitemid 39079838)
22. Doherty E.S., Lacbawan F., Hadley D.W., et al. Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature. Am J Med Genet A. 2007;143A(24):3204-3215. (Pubitemid 350274837)
23. Honnebier M.B., Cabiling D.S., Hetlinger M., McDonald-McGinn D.M., Zackai E.H., Bartlett S.P. The natural history of patients treated for FGFR3-associated (Muenketype) craniosynostosis. Plast Reconstr Surg. 2008;121(3):919-931. (Pubitemid 351642826)
24. Mansour S.L., Twigg S.R., Freeland R.M., Wall S.A., Li C., Wilkie A.O. Hearing loss in a mouse model of Muenke syndrome. Hum Mol Genet. 2009;18(1):43-50.
25. Elfenbein J.L., Waziri M., Morris H.L. Verbal communication skills of six children with craniofacial anomalies. Cleft Palate J. 1981;18(1):59-64. (Pubitemid 11183505)