Etiology of unilateral hearing loss in a national hereditary deafness repository

American Journal of Otolaryngology - Head and Neck Medicine and Surgery

Volumn 33, Issue 5, 2012, Pages 590-594

  Dodson, Kelley M ^a   Georgolios, Alexandros ^a   Barr, Noelle ^a   Nguyen, Bich ^b   Sismanis, Aristides ^a   Arnos, Kathleen S ^c   Norris, Virginia W ^c   Chapman, Derek ^a   Nance, Walter E ^a   Pandya, Arti ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^b University of Missouri   (United States)

^c GALLAUDET UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; CONNEXIN 31;

ADOLESCENT; ADULT; AFRICAN AMERICAN; ARTICLE; AUDIOLOGY; CHILD; CLINICAL ARTICLE; CLINICAL DATA REPOSITORY; COCH GENE; EAR; EAR DYSPLASIA; EAR MALFORMATION; FAMILY HISTORY; FEMALE; GENE; GENE INTERACTION; GENE MUTATION; GENE SEQUENCE; GENETIC TRAIT; HISPANIC; HUMAN; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; SCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM; TECTA GENE; UNILATERAL HEARING LOSS; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CONNEXINS; DEAFNESS; DNA; FEMALE; FOLLOW-UP STUDIES; GENETIC TESTING; GENOTYPE; HEARING; HEARING LOSS, UNILATERAL; HUMANS; INFANT; MALE; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84865680640     PISSN: 01960709     EISSN: 1532818X     Source Type: Journal    
DOI: 10.1016/j.amjoto.2012.03.005     Document Type: Article

References (24)

1. C.C. Morton, and W.E. Nance Newborn hearing screening - a silent revolution N Engl J Med 354 2006 2151 2164
2. M.L. Marazita, L.M. Ploughman, and B. Rawlings Genetic epidemiological studies of early-onset deafness in the U.S. school-age population Am J Med Genet 46 1993 486 491
3. J.E. Lieu Speech-language and educational consequences of unilateral hearing loss in children Arch Otolaryngol Head Neck Surg 130 2004 524 530
4. J.E. Widen, R.C. Folsom, and B. Cone-Wesson Identification of neonatal hearing impairment: hearing status at 8 to 12 months corrected age using a visual reinforcement audiometry protocol Ear Hear 21 2000 471 487
5. A.L. Mehl, and V. Thomson Newborn hearing screening: the great omission Pediatrics 101 1998 E4
6. T. Finitzo, K. Albright, and J. O'Neal The newborn with hearing loss: detection in the nursery Pediatrics 102 1998 1452 1460
7. L. Barsky-Firkser, and S. Sun Universal newborn hearing screenings: a three-year experience Pediatrics 99 1997 E4
8. G. Everberg Etiology of unilateral total deafness studied in a series of children and young adults Ann Otol Rhinol Laryngol 69 1960 711 730
9. A.S. Niskar, S.M. Kieszak, and A. Holmes Prevalence of hearing loss among children 6 to 19 years of age: the Third National Health and Nutrition Examination Survey JAMA 279 1998 1071 1075
10. D.A. Chapman, C.C. Stampfel, and J.N. Bodurtha The impact of co-occurring birth defects on the timing of newborn hearing screening and diagnosis Am J Audiol 2011
11. K.M. Dodson, T. Kamei, and A. Sismanis Familial unilateral deafness and delayed endolymphatic hydrops Am J Med Genet A 143 2007 1661 1665
12. G. Everberg Further studies on hereditary unilateral deafness Acta Otolaryngol 51 1960 615 635
13. P.E. Brookhouser, D.W. Worthington, and W.J. Kelly Unilateral hearing loss in children Laryngoscope 101 1991 1264 1272
14. K.M. Dodson, A. Sismanis, and W.E. Nance Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness Am J Med Genet A 130 2004 22 25
15. S.A. Ross, Z. Novak, and R.A. Kumbla GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection Pediatr Res 2007
16. G.I. Bell, J.H. Karam, and W.J. Rutter region adjacent to the 5′ end of the human insulin gene Proc Natl Acad Sci U S A 78 1981 5759 5763
17. A. Pandya, X. Xia, and J. Radnaabazar Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity J Med Genet 34 1997 169 172
18. X.Z. Liu, X.J. Xia, and L.R. Xu Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss Hum Mol Genet 9 2000 63 67
19. K. Verhoeven, L. Van Laer, and K. Kirschhofer Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Nat Genet 19 1998 60 62
20. M. Mustapha, D. Weil, and S. Chardenoux An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21 Hum Mol Genet 8 1999 409 412
21. T. Yang, H. Vidarsson, and S. Rodrigo-Blomqvist Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4) Am J Hum Genet 80 2007 1055 1063
22. N.G. Robertson, L. Lu, and S. Heller Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction Nat Genet 20 1998 299 303
23. J.J. Song, H.G. Choi, and S.H. Oh Unilateral sensorineural hearing loss in children: the importance of temporal bone computed tomography and audiometric follow-up Otol Neurotol 30 2009 604 608
24. E. Liepinsh, M. Trexler, and A. Kaikkonen NMR structure of the LCCL domain and implications for DFNA9 deafness disorder EMBO J 20 2001 5347 5353