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Volumn 35, Issue 2, 2006, Pages 221-225

Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss

Author keywords

Congenital cytomegalovirus infections; EHDI; Pre lingual deafness

Indexed keywords

GAP JUNCTION PROTEIN;

EID: 30144441419     PISSN: 13866532     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcv.2005.09.017     Document Type: Conference Paper
Times cited : (119)

References (39)
  • 1
    • 30144442035 scopus 로고    scopus 로고
    • Dried blood spot PCR to screen newborns for congenital cytomegalovirus infection
    • G. Ashrith, Z. Novak, and S.A. Brice Dried blood spot PCR to screen newborns for congenital cytomegalovirus infection Soc Pediat Res Abstract 2004
    • (2004) Soc Pediat Res Abstract
    • Ashrith, G.1    Novak, Z.2    Brice, S.A.3
  • 3
    • 0842326741 scopus 로고    scopus 로고
    • Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both 35delG of GJB2 and the 342-kb deletion involving GJB6
    • H. Bolz, G. Schade, S. Ehmer, C. Kothe, M. Hess, and A. Gal Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both 35delG of GJB2 and the 342-kb deletion involving GJB6 Hear Res 188 2004 42 46
    • (2004) Hear Res , vol.188 , pp. 42-46
    • Bolz, H.1    Schade, G.2    Ehmer, S.3    Kothe, C.4    Hess, M.5    Gal, A.6
  • 4
    • 18544371057 scopus 로고    scopus 로고
    • Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness
    • Y. Bykhovskya, Y. Yang, K. Taylor, T. Hang, R.Y. Tun, and X. Estivill Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness Genet Med 3 2001 177 180
    • (2001) Genet Med , vol.3 , pp. 177-180
    • Bykhovskya, Y.1    Yang, Y.2    Taylor, K.3    Hang, T.4    Tun, R.Y.5    Estivill, X.6
  • 5
    • 0035034863 scopus 로고    scopus 로고
    • Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations
    • C. Campbell, R.A. Cucci, S. Prasad, G.E. Green, J.B. Edeal, and C.E. Galer Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations Hum Mutat 17 2001 403 411
    • (2001) Hum Mutat , vol.17 , pp. 403-411
    • Campbell, C.1    Cucci, R.A.2    Prasad, S.3    Green, G.E.4    Edeal, J.B.5    Galer, C.E.6
  • 6
    • 0037046804 scopus 로고    scopus 로고
    • Targeted ablation of Connexin 26 in the inner ear epithelial gap junction network causes hearing impairment and cell death
    • M. Cohen-Salmon, T. Ott, V. Michel, J.-P. Hardelin, I. Perfettini, and M. Eybalin Targeted ablation of Connexin 26 in the inner ear epithelial gap junction network causes hearing impairment and cell death Curr Biol 12 2002 1106 1111
    • (2002) Curr Biol , vol.12 , pp. 1106-1111
    • Cohen-Salmon, M.1    Ott, T.2    Michel, V.3    Hardelin, J.-P.4    Perfettini, I.5    Eybalin, M.6
  • 7
    • 0042828920 scopus 로고    scopus 로고
    • Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
    • F.J. del Castillo, M. Rodriguez-Ballesteros, Y. Martin, B. Arellano, J. Gallo-Teran, and C. Morales-Angulo Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss J Med Genet 40 2003 632 636
    • (2003) J Med Genet , vol.40 , pp. 632-636
    • Del Castillo, F.J.1    Rodriguez-Ballesteros, M.2    Martin, Y.3    Arellano, B.4    Gallo-Teran, J.5    Morales-Angulo, C.6
  • 8
    • 0033577528 scopus 로고    scopus 로고
    • Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: Implications for genetic counseling
    • F. Denoyelle, S. Marlin, and D. Weil Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counseling Lancet 353 1999 1298 1303
    • (1999) Lancet , vol.353 , pp. 1298-1303
    • Denoyelle, F.1    Marlin, S.2    Weil, D.3
  • 9
    • 85030352519 scopus 로고    scopus 로고
    • The efficacy of early identification and intervention for children with hearing impairment
    • M. Down, and C. Yoshinago-Itano The efficacy of early identification and intervention for children with hearing impairment Pediat Clin N America 46 1999 352 357
    • (1999) Pediat Clin N America , vol.46 , pp. 352-357
    • Down, M.1    Yoshinago-Itano, C.2
  • 10
    • 17344365276 scopus 로고    scopus 로고
    • Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
    • X. Estivill, N. Govea, E. Barcelo, C. Badanas, E. Romero, and L. Moral Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides Am J Hum Genet 62 1998 27 35
    • (1998) Am J Hum Genet , vol.62 , pp. 27-35
    • Estivill, X.1    Govea, N.2    Barcelo, E.3    Badanas, C.4    Romero, E.5    Moral, L.6
  • 12
    • 0035828440 scopus 로고    scopus 로고
    • Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: Questionnaire based ascertainment study
    • H.M. Fortnum, A.Q. Summerfield, D.H. Marshall, A.C. Davis, and J.M. Bamford Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study BMJ 323 2001 1 6
    • (2001) BMJ , vol.323 , pp. 1-6
    • Fortnum, H.M.1    Summerfield, A.Q.2    Marshall, D.H.3    Davis, A.C.4    Bamford, J.M.5
  • 13
    • 0030812608 scopus 로고    scopus 로고
    • Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection
    • K.B. Fowler, F.P. McCollister, A.J. Dahle, S. Boppana, and R.F. Pass Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection J Pediat 130 1997 624 630
    • (1997) J Pediat , vol.130 , pp. 624-630
    • Fowler, K.B.1    McCollister, F.P.2    Dahle, A.J.3    Boppana, S.4    Pass, R.F.5
  • 14
    • 0033511445 scopus 로고    scopus 로고
    • Newborn hearing screening: Will children with hearing loss caused by congenital cytomegalovirus infection be missed?
    • K.B. Fowler, A.J. Dahle, S.B. Boppana, and R.F. Pass Newborn hearing screening: will children with hearing loss caused by congenital cytomegalovirus infection be missed? J Pediatr 135 1999 60 64
    • (1999) J Pediatr , vol.135 , pp. 60-64
    • Fowler, K.B.1    Dahle, A.J.2    Boppana, S.B.3    Pass, R.F.4
  • 15
    • 0346154518 scopus 로고
    • Association of congenital deafness with goiter (Pendred syndrome): A study of 107 families
    • G.R. Fraser Association of congenital deafness with goiter (Pendred syndrome): a study of 107 families Ann Hum Genet 28 1965 201 249
    • (1965) Ann Hum Genet , vol.28 , pp. 201-249
    • Fraser, G.R.1
  • 17
    • 0037959640 scopus 로고    scopus 로고
    • Lack of pendren expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice
    • M. Hulander, A.E. Kiernan, S.R. Blomquist, P. Carisson, E.-J. Samuelsson, and B.R. Johansson Lack of pendren expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice Development 130 2003 2013 2025
    • (2003) Development , vol.130 , pp. 2013-2025
    • Hulander, M.1    Kiernan, A.E.2    Blomquist, S.R.3    Carisson, P.4    Samuelsson, E.-J.5    Johansson, B.R.6
  • 18
    • 0025405788 scopus 로고
    • Audiometric accuracy of the click ABR in infants at risk for hearing loss
    • M.L. Hyde, K. Riko, and K. Malizia Audiometric accuracy of the click ABR in infants at risk for hearing loss J Am Acad Audiol 1 1990 59 66
    • (1990) J Am Acad Audiol , vol.1 , pp. 59-66
    • Hyde, M.L.1    Riko, K.2    Malizia, K.3
  • 19
    • 0033834029 scopus 로고    scopus 로고
    • Year 2000 position statement: Principals and guidelines for early hearing detection and intervention programs
    • Joint Committee on Infant Hearing
    • Joint Committee on Infant Hearing Year 2000 position statement: principals and guidelines for early hearing detection and intervention programs Am J Audiol 9 2000 9 29
    • (2000) Am J Audiol , vol.9 , pp. 9-29
  • 20
    • 4444275884 scopus 로고    scopus 로고
    • Universal neonatal hearing screening moving from evidence to practice
    • C. Kennedy, and D. McCann Universal neonatal hearing screening moving from evidence to practice Arch Dis Child Fetal Neonatal Ed 89 2004 F378 F383
    • (2004) Arch Dis Child Fetal Neonatal Ed , vol.89
    • Kennedy, C.1    McCann, D.2
  • 21
    • 0042243568 scopus 로고    scopus 로고
    • Effect of ganciclovir therapy on hearing in symptomatic congenital cytomegalovirus disease involving the central nervous system: A randomized, controlled trial
    • D.W. Kimberlin, C.-Y. Lin, P.J. Sanchez, G.J. Demmler, W. Danker, and M. Shelton Effect of ganciclovir therapy on hearing in symptomatic congenital cytomegalovirus disease involving the central nervous system: a randomized, controlled trial J Pediatr 143 2003 16 25
    • (2003) J Pediatr , vol.143 , pp. 16-25
    • Kimberlin, D.W.1    Lin, C.-Y.2    Sanchez, P.J.3    Demmler, G.J.4    Danker, W.5    Shelton, M.6
  • 24
    • 0033064890 scopus 로고    scopus 로고
    • Prevalence and characteristics of children with serious hearing impairment in metropolitan Atlanta, 1991-1993
    • K.V. Naarden, P. Decoufle, and K. Caldwell Prevalence and characteristics of children with serious hearing impairment in metropolitan Atlanta, 1991-1993 Pediatrics 103 1999 570 575
    • (1999) Pediatrics , vol.103 , pp. 570-575
    • Naarden, K.V.1    Decoufle, P.2    Caldwell, K.3
  • 26
    • 0031055387 scopus 로고    scopus 로고
    • Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
    • A. Pandya, X. Xia, J. Radnaabazar, J. Batsuuri, B. Dangaasuren, and N. Fischel-Ghodsian Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity J Med Genet 34 1997 169 172
    • (1997) J Med Genet , vol.34 , pp. 169-172
    • Pandya, A.1    Xia, X.2    Radnaabazar, J.3    Batsuuri, J.4    Dangaasuren, B.5    Fischel-Ghodsian, N.6
  • 27
    • 10744224474 scopus 로고    scopus 로고
    • Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands
    • A. Pandya, K.S. Arnos, and W.E. Nance Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands Genet Med 5 2003 295 303
    • (2003) Genet Med , vol.5 , pp. 295-303
    • Pandya, A.1    Arnos, K.S.2    Nance, W.E.3
  • 28
    • 0023575680 scopus 로고
    • Congenital cytomegalovirus infection: A cause of sensorineural hearing loss
    • C.S. Peckham, O. Stark, J.A. Dudgeon, J.A. Martin, and G. Hawkins Congenital cytomegalovirus infection: a cause of sensorineural hearing loss Arch Dis Child 62 1987 1233 1237
    • (1987) Arch Dis Child , vol.62 , pp. 1233-1237
    • Peckham, C.S.1    Stark, O.2    Dudgeon, J.A.3    Martin, J.A.4    Hawkins, G.5
  • 29
    • 9644287853 scopus 로고    scopus 로고
    • A diagnostic paradigm for childhood idiopathic sensorineural hearing loss
    • D.A. Preciado, L.H. Lim, and A.P. Cohen A diagnostic paradigm for childhood idiopathic sensorineural hearing loss Otolaryngol Head Neck Surg 131 2004 804 809
    • (2004) Otolaryngol Head Neck Surg , vol.131 , pp. 804-809
    • Preciado, D.A.1    Lim, L.H.2    Cohen, A.P.3
  • 30
    • 13444254030 scopus 로고    scopus 로고
    • SCL26A/PDS: Evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities
    • S.P. Pryor, A.C. Madeo, J.C. Reynolds, N.J. Sarlis, K.S. Arnos, and W.E. Nance SCL26A/PDS: evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities J Med Genet 42 2005 159 165
    • (2005) J Med Genet , vol.42 , pp. 159-165
    • Pryor, S.P.1    Madeo, A.C.2    Reynolds, J.C.3    Sarlis, N.J.4    Arnos, K.S.5    Nance, W.E.6
  • 32
    • 0034753362 scopus 로고    scopus 로고
    • At the speed of sound: Gene discovery in the auditory system
    • B.L. Resendes, R.E. Williamson, and C.C. Morton At the speed of sound: gene discovery in the auditory system Am J Hum Genet 69 2001 923 935
    • (2001) Am J Hum Genet , vol.69 , pp. 923-935
    • Resendes, B.L.1    Williamson, R.E.2    Morton, C.C.3
  • 33
    • 0035968605 scopus 로고    scopus 로고
    • Advances in hereditary deafness
    • M. Tekin, K.S. Arnos, and A. Pandya Advances in hereditary deafness Lancet 358 2001 1082 1090
    • (2001) Lancet , vol.358 , pp. 1082-1090
    • Tekin, M.1    Arnos, K.S.2    Pandya, A.3
  • 35
    • 0031682552 scopus 로고    scopus 로고
    • The Rhode Island hearing assessment program: Experience with statewide hearing screening (1993-1996)
    • B.R. Vohr, L.M. Carty, and P.E. Moore The Rhode Island hearing assessment program: experience with statewide hearing screening (1993-1996) J Pediatr 133 1998 353 357
    • (1998) J Pediatr , vol.133 , pp. 353-357
    • Vohr, B.R.1    Carty, L.M.2    Moore, P.E.3
  • 36
    • 0037642358 scopus 로고    scopus 로고
    • The current status of EHDI programs in the United States
    • K.R. White The current status of EHDI programs in the United States Ment Retard Dev Disabil Res Rev 9 2003 79 88
    • (2003) Ment Retard Dev Disabil Res Rev , vol.9 , pp. 79-88
    • White, K.R.1
  • 38
    • 0347382300 scopus 로고    scopus 로고
    • Early intervention after universal neonatal hearing screening: Impact on outcomes
    • C. Yoshinaga-Itano Early intervention after universal neonatal hearing screening: impact on outcomes Ment Retard Dev Disabil Res Rev 2003 252 266
    • (2003) Ment Retard Dev Disabil Res Rev , pp. 252-266
    • Yoshinaga-Itano, C.1
  • 39
    • 0347003512 scopus 로고    scopus 로고
    • Maternally inherited aminoglycoside-induced and non-syndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family
    • H. Zhao, R. Li, Q. Wang, O. Yan, J.H. Deng, and D. Han Maternally inherited aminoglycoside-induced and non-syndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family Am J Hum Genet 74 2004 139 152
    • (2004) Am J Hum Genet , vol.74 , pp. 139-152
    • Zhao, H.1    Li, R.2    Wang, Q.3    Yan, O.4    Deng, J.H.5    Han, D.6


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