|
1
|
Nieman CL and McMahon CM: The World Health
Organization's world report on hearing: A call to action for
hearing care providers. J Laryngol Otol. 134:377–378.
2020.PubMed/NCBI View Article : Google Scholar
|
|
2
|
Fortnum HM, Summerfield AQ, Marshall DH,
Davis AC and Bamford JM: Prevalence of permanent childhood hearing
impairment in the United Kingdom and implications for universal
neonatal hearing screening: Questionnaire based ascertainment
study. BMJ. 323:536–540. 2001.PubMed/NCBI View Article : Google Scholar
|
|
3
|
Kennedy C and McCann D: Universal neonatal
hearing screening moving from evidence to practice. Arch Dis Child
Fetal Neonatal Ed. 89:F378–F383. 2004.PubMed/NCBI View Article : Google Scholar
|
|
4
|
Tobe RG, Mori R, Huang L, Xu L, Han D and
Shibuya K: Cost-effectiveness analysis of a national neonatal
hearing screening program in China: Conditions for the scale-up.
PLoS One. 8(e51990)2013.PubMed/NCBI View Article : Google Scholar
|
|
5
|
Huang LH, Zhang L, Tobe RY, Qi FH, Sun L,
Teng Y, Ke QL, Mai F, Zhang XF, Zhang M, et al: Cost-effectiveness
analysis of neonatal hearing screening program in China: Should
universal screening be prioritized? BMC Health Serv Res.
12(97)2012.PubMed/NCBI View Article : Google Scholar
|
|
6
|
Young NM, Reilly BK and Burke L:
Limitations of universal newborn hearing screening in early
identification of pediatric cochlear implant candidates. Arch
Otolaryngol Head Neck Surg. 137:230–234. 2011.PubMed/NCBI View Article : Google Scholar
|
|
7
|
Morton CC and Nance WE: Newborn hearing
screening-a silent revolution. N Engl J Med. 354:2151–2164.
2006.PubMed/NCBI View Article : Google Scholar
|
|
8
|
Wang Q, Xiang J, Sun J, Yang Y, Guan J,
Wang D, Song C, Guo L, Wang H, Chen Y, et al: Nationwide population
genetic screening improves outcomes of newborn screening for
hearing loss in China. Genet Med. 21:2231–2238. 2019.PubMed/NCBI View Article : Google Scholar
|
|
9
|
Tang X, Liu L, Liang S, Liang M, Liao T,
Luo S, Yan T and Chen J: Concurrent newborn hearing and genetic
screening in a Multi-ethnic population in South China. Front
Pediatr. 9(734300)2021.PubMed/NCBI View Article : Google Scholar
|
|
10
|
Barendregt JJ, Doi SA, Lee YY, Norman RE
and Vos T: Meta-analysis of prevalence. J Epidemiol Community
Health. 67:974–978. 2013.PubMed/NCBI View Article : Google Scholar
|
|
11
|
Yáñez-Baeza C, Aguilera-Eguía RA,
Fuentes-Barría H and Roco-Videla Á: Importance of the PRISMA
guideline. Nutr Hosp. 40:670–675. 2023.PubMed/NCBI View Article : Google Scholar : (In Spanish).
|
|
12
|
Zhu QW, Li MT, Zhuang X, Chen K, Xu WQ,
Jiang YH and Qin G: Assessment of hearing screening combined with
limited and expanded genetic screening for newborns in Nantong,
China. JAMA Netw Open. 4(e2125544)2021.PubMed/NCBI View Article : Google Scholar
|
|
13
|
Zeng X, Liu Z, Wang J and Zeng X: Combined
hearing screening and genetic screening of deafness among Hakka
newborns in China. Int J Pediatr Otorhinolaryngol.
136(110120)2020.PubMed/NCBI View Article : Google Scholar
|
|
14
|
Egger M, Davey Smith G, Schneider M and
Minder C: Bias in meta-analysis detected by a simple, graphical
test. BMJ. 315:629–634. 1997.PubMed/NCBI View Article : Google Scholar
|
|
15
|
Wang QJ, Zhao YL, Rao SQ, Guo YF, He Y,
Lan L, Yang WY, Zheng QY, Ruben RJ, Han DY and Shen Y: Newborn
hearing concurrent gene screening can improve care for hearing
loss: A study on 14,913 Chinese newborns. Int J Pediatr
Otorhinolaryngol. 75:535–542. 2011.PubMed/NCBI View Article : Google Scholar
|
|
16
|
Zhang Z, Ding W, Liu X, Xu B, Du W, Nan S
and Guo Y: Auditory screening concurrent deafness predisposing
genes screening in 10,043 neonates in Gansu province, China. Int J
Pediatr Otorhinolaryngol. 76:984–988. 2012.PubMed/NCBI View Article : Google Scholar
|
|
17
|
Zhang J, Wang P, Han B, Ding Y, Pan L, Zou
J, Liu H, Pang X, Liu E, Wang H, et al: Newborn hearing concurrent
genetic screening for hearing impairment-a clinical practice in
58,397 neonates in Tianjin, China. Int J Pediatr Otorhinolaryngol.
77:1929–1935. 2013.PubMed/NCBI View Article : Google Scholar
|
|
18
|
Peng Q, Huang S, Liang Y, Ma K, Li S, Yang
L, Li W, Ma Q, Liu Q, Zhong B and Lu X: Concurrent genetic and
standard screening for hearing impairment in 9317 Southern Chinese
Newborns. Genet Test Mol Biomarkers. 20:603–608. 2016.PubMed/NCBI View Article : Google Scholar
|
|
19
|
Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH,
Huang FL, Tsao PN, Su YN, Lee YL, Hsieh WS and Hsu CJ: Newborn
genetic screening for hearing impairment: A population-based
longitudinal study. Genet Med. 19:6–12. 2017.PubMed/NCBI View Article : Google Scholar
|
|
20
|
Lu CY, Tsao PN, Ke YY, Lin YH, Lin YH,
Hung CC, Su YN, Hsu WC, Hsieh WS, Huang LM, et al: Concurrent
hearing, genetic, and cytomegalovirus screening in Newborns,
Taiwan. J Pediatr. 199:144–50.e1. 2018.PubMed/NCBI View Article : Google Scholar
|
|
21
|
Dai P, Huang LH, Wang GJ, Gao X, Qu CY,
Chen XW, Ma FR, Zhang J, Xing WL, Xi SY, et al: Concurrent hearing
and genetic screening of 180,469 neonates with Follow-up in
Beijing, China. Am J Hum Genet. 105:803–812. 2019.PubMed/NCBI View Article : Google Scholar
|
|
22
|
Luo H, Yang Y, Wang X, Xu F, Huang C, Liu
D, Zhang L, Huang T, Ma P, Lu Q, et al: Concurrent newborn hearing
and genetic screening of common hearing loss variants with
bloodspot-based targeted next generation sequencing in Jiangxi
province. Front Pediatr. 10(1020519)2022.PubMed/NCBI View Article : Google Scholar
|
|
23
|
Wen C, Yang X, Cheng X, Zhang W, Li Y,
Wang J, Wang C, Ruan Y, Zhao L, Lu H, et al: Optimized concurrent
hearing and genetic screening in Beijing, China: A cross-sectional
study. Biosci Trends. 17:148–159. 2023.PubMed/NCBI View Article : Google Scholar
|
|
24
|
Wang QJ, Zhao YL, Lan L, Zhao C, Han MK
and Han DY: Studies of the strategy for newborn gene screening.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 42:809–813.
2007.PubMed/NCBI(In Chinese).
|
|
25
|
D'Aguillo C, Bressler S, Yan D, Mittal R,
Fifer R, Blanton SH and Liu X: Genetic screening as an adjunct to
universal newborn hearing screening: Literature review and
implications for non-congenital pre-lingual hearing loss. Int J
Audiol. 58:834–850. 2019.PubMed/NCBI View Article : Google Scholar
|
|
26
|
Nivoloni Kde A, da Silva-Costa SM, Pomilio
MC, Pereira T, Lopes Kde C, de Moraes VC, Alexandrino F, de
Oliveira CA and Sartorato EL: Newborn hearing screening and genetic
testing in 8974 Brazilian neonates. Int J Pediatr Otorhinolaryngol.
74:926–929. 2010.PubMed/NCBI View Article : Google Scholar
|
|
27
|
Han B, Zong L, Li Q, Zhang Z, Wang D, Lan
L, Zhang J, Zhao Y and Wang Q: Newborn genetic screening for high
risk deafness-associated mutations with a new Tetra-primer ARMS PCR
kit. Int J Pediatr Otorhinolaryngol. 77:1440–1445. 2013.PubMed/NCBI View Article : Google Scholar
|
|
28
|
Guo L, Xiang J, Sun L, Yan X, Yang J, Wu
H, Guo K, Peng J, Xie X, Yin Y, et al: Concurrent hearing and
genetic screening in a general newborn population. Hum Genet.
139:521–530. 2020.PubMed/NCBI View Article : Google Scholar
|
