Progressive or delayed early-onset pediatric sensorineural hearing loss

Journal of Otolaryngology of Japan

Volumn 114, Issue 6, 2011, Pages 557-561

  Kataoka, Yuko ^a   Fukushima, Kunihiro ^a   Maeda, Yukihide ^a   Sugaya, Akiko ^a   Nagayasu, Rie ^a   Masuda, Yu ^b   Nishizaki, Kazunori ^a  

^a OKAYAMA UNIVERSITY   (Japan)

^b Okayama Kanariya Gakuen   (Japan)

Author keywords

Cochlear implant; Delayed onset hearing loss; Newborn hearing screening enlarged vestibular aqueduct; Progressive hearing loss

Indexed keywords

EID: 79960912839     PISSN: 00306622     EISSN: None     Source Type: Journal    
DOI: 10.3950/jibiinkoka.114.557     Document Type: Article

References (19)

1. Fukushima K, Mimaki N, Fukuda S, et al: Pilot study of universal newborn hearing screening in Japan: districtbased screening program in Okayama. Ann Otol Rhinol Laryngol 2008;117:166-171. (Pubitemid 351415350)
2. Newton VE, Rowson VJ: Progressive sensorineural hearing loss in childhood. Br J Audiol 1988;22:287-295. (Pubitemid 19030830)
3. Walch C, Anderhuber W, Kole W, et al: Bilateral sensorineural hearing disorders in children: etiology of deafness and evaluation of hearing tests, Int J Pediatr Otorhinolaryngol 2000;53:31-38. (Pubitemid 30336258)
4. Berrettini S, Ravecca F, Sellari-Franceshini S, et al: Progressive sensorineural hearing loss in children. Pediatr Neurol 1999;20:130-136. (Pubitemid 29102613)
5. Joint Committee on Infant Hearing: Year 2007 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention Programs. Pediarics 2007;120:898-921.
6. Haritani S, Tanaka Y: Changes in hearing ability after neonatal hearing screening. Audiology Japan 2005;48:196-204.
7. Usami S, Abe S, Weston MD, et al: Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations. Hum Genet 1999;104:117-200.
8. Gorlin RJ: Genetic hearing loss associated with endocrine and metabolic disorders. Hereditary hearing loss and its syndromes. Gorlin RJ, Toriello HV, Cohen MM (eds). Oxford Univ Pr; 1995: pp 337-339.
9. Zalzal GH, Tomoski SM, Veniza LG, et al: Enlarged vestibular aqueduct and sensorineural hearing loss in children. Arch Otolaryngol Head Neck Surg 1995;121:23-28.
10. Govaert PJ, Casselman J, Daemers K. et al: Audiological findings in large vestibular aqueduct syndrome, Int J Pediatr Otorhinolaryngol 1999;5:157-164.
11. Swartz JD: An overview of congenital/development sensorineural hearing loss with emphasis on the vestibular aqueduct. Semin ultrasound CT MR 2004;25:353-368.
12. Trimble K, Blaser S, James AL, et al: Computed tomography and/or magnetic resonance imaging before pediatric cochlear implantation? Developing an investigative strategy. Otol Neurotol 2007;28:317-324. (Pubitemid 46607901)
13. Donnelly LF, Frush DP: Pediatric multidetector body CT. Radiol Clin North Am 2003;41:637-655. (Pubitemid 36597531)
14. Nie L: KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss. Curr Opin Otolaryngol Head Neck Surg 2008;16:441-444.
15. Bork JM, Peters LM, Riazuddin S, et al: Usher syndrome ID and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 2001;68:26-37. (Pubitemid 32048359)
16. Usami S, Abe S, Akita J, et al: Prevalence of mitochondrial gene mutations among hearing impaired patients. J Med Genet 2000;37:38-40. (Pubitemid 30245872)
17. Pagarkar W, Britner-Glindziez M, Knight J, et al: Late postnatal onset of hearing loss due to GJB2 mutations, Int J Pediatr Otorhinolaryngol 2006;70:1119-1124. (Pubitemid 44389607)
18. Norris VW, Arnos KS, Hanks WD, et al: Does universal newborn hearing screening identify all children with GJB 2 (Connexin 26) deafness? Penetrance of GJB2 deafness. Ear Hear 2006;27:732-741. (Pubitemid 44691233)
19. Fowler KB, Dahle AJ, Bopana SB, et al: Newborn hearing screening: Will children with hearing loss caused congenital cytomegalovirus infection be missed? Journal of pediatrics 1999;135:60-64. (Pubitemid 30180563)