Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueducts

Archives of Otolaryngology - Head and Neck Surgery

Volumn 131, Issue 5, 2005, Pages 388-392

  Pryor, Shannon P ^a   Demmler, Gail J ^b   Madeo, Anne C ^a   Yang, Yandan ^a   Zalewski, Chris K ^a   Brewer, Carmen C ^a   Butman, John A ^c   Fowler, Karen B ^d   Griffith, Andrew J ^a  

^a NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOMEGALOVIRUS ANTIBODY;

ADOLESCENT; ADULT; ARTICLE; AUDIOMETRY; CHILD; CONGENITAL INFECTION; CYTOMEGALOVIRUS INFECTION; DISEASE ASSOCIATION; DISEASE COURSE; GENE MUTATION; HUMAN; INFANT; MAJOR CLINICAL STUDY; ONSET AGE; PENDRED SYNDROME; PERCEPTION DEAFNESS; PREVALENCE; SEROPREVALENCE; VESTIBULAR DISORDER; VESTIBULE AQUEDUCT;

ADOLESCENT; AUDIOMETRY; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; CYTOMEGALOVIRUS INFECTIONS; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MUTATION; VESTIBULAR AQUEDUCT;

EID: 18344391730     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.131.5.388     Document Type: Article

References (26)

1. Valvassori GE, Clemis JD. The large vestibular aqueduct syndrome. Laryngoscope. 1978;88:723-728.
2. Jackler RK, De La Cruz A. The large vestibular aqueduct syndrome. Laryngoscope. 1989;99:1238-1242.
3. Griffith AJ, Arts A, Downs C, et al. Familial large vestibular aqueduct syndrome. Laryngoscope. 1996;106:960-965.
4. Madden C, Halsted M, Benton C, Greinwald J, Choo D. Enlarged vestibular aqueduct syndrome in the pediatric population. Otol Neurotol. 2003;24:625-632.
5. Everett LA, Glaser B, Beck JC, et al. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet. 1997;17:411-422.
6. Li XC, Everett LA, Lalwani AK, et al. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet. 1998;18:215-217.
7. Park HJ, Shaukat S, Liu XZ, et al. Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness. J Med Genet. 2003;40:242-248.
8. Pryor S, Madeo A, Reynolds J, et al. SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and nonsyndromic EVA are distinct clinical and genetic entities. J Med Genet. 2005;42:159-165.
9. Park HJ, Lee SJ, Jin HS, et al. Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans. Clin Genet. 2005;67:160-165.
10. Bauman NM, Kirby-Keyser LJ, Dolan KD, et al. Mondini dysplasia and congenital cytomegalovirus infection. J Pediatr. 1994;124:71-78.
11. Myers EN, Stool S. Cytomegalic inclusion disease of the inner ear. Laryngoscope. 1968;78:1904-1915.
12. Davis LE, Johnsson LG, Kornfeld M. Cytomegalovirus labyrinthitis in an infant: morphological, virological, and immunofluorescent studies. J Neuropathol Exp Neurol. 1981;40:9-19.
13. Everett LA, Morsli H, Wu DK, Green ED. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc Natl Acad Sci U S A. 1999;96:9727-9732.
14. Stagno S, Reynolds DW, Huang ES, Thames SD, Smith RJ, Alford CA. Congenital cytomegalovirus infection. N Engl J Med. 1977;296:1254-1258.
15. Yow MD, Williamson DW, Leeds U, et al. Epidemiologic characteristics of cytomegalovirus infection in mothers and their infants. Am J Obstet Gynecol. 1988;158:1189-1195.
16. Fowler KB, Dahle AJ, Boppana SB, Pass RF. Newborn hearing screening: will children with hearing loss caused by congenital cytomegalovirus infection be missed? J Pediatr. 1999;135:60-64.
17. Demmler GJ. Infectious Diseases Society of America and Centers for Disease Control: summary of a workshop on surveillance for congenital cytomegalovirus disease. Rev Infect Dis. 1991;13:315-329.
18. Pass RF, Stagno S, Myers GJ, Alford CA. Outcome of symptomatic congenital cytomegalovirus infection: results of long-term longitudinal follow-up. Pediatrics. 1980;66:758-762.
19. Dahle AJ, Fowler KB, Wright JD, Boppana SB, Britt WJ, Pass RF. Longitudinal investigation of hearing disorders in children with congenital cytomegalovirus. J Am Acad Audiol. 2000;11:283-290.
20. Barbi M, Binda S, Caroppo S, Ambrosetti U, Corbetta C, Sergi P. A wider role for congenital cytomegalovirus infection in sensorineural hearing loss. Pediatr Infect Dis J. 2003;22:39-42.
21. Williamson WD, Demmler GJ, Percy AK, Catlin FI. Progressive hearing loss in infants with asymptomatic congenital cytomegalovirus infection. Pediatrics. 1992;90:862-866.
22. Fowler KB, McCollister FP, Dahle AJ, Boppana S, Britt WJ, Pass RF. Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection. J Pediatr. 1997;130:624-630.
23. Huygen PL, Admiraal RJ. Audiovestibular sequelae of congenital cytomegalovirus infection in 3 children presumably representing 3 symptomatically different types of delayed endolymphatic hydrops. Int J Pediatr Otorhinolaryngol. 1996;35:143-154.
24. Pappas DG. Hearing impairments and vestibular abnormalities among children with subclinical cytomegalovirus. Ann Otol Rhinol Laryngol. 1983;92:552-557.
25. European Working Group on Genetics of Hearing Impairment. Infoletter. Available at: http://wvw2.unife.it/gendeaf/hear/infoletters/Info_02.PDF. Accessed March 16, 2005.
26. de Jong MD, Galasso GJ, Gazzard B, et al. Summary of the II International Symposium on Cytomegalovirus. Antiviral Res. 1998;39:141-162.