山东大学耳鼻喉眼学报 ›› 2022, Vol. 36 ›› Issue (1): 131-137.doi: 10.6040/j.issn.1673-3770.0.2021.080

• 研究进展 • 上一篇    下一篇

新生儿听力障碍常见危险因素及听力筛查方法研究进展

盘琳琳,孔令漪,翟丰,陈洁   

  1. 上海交通大学医学院附属上海儿童医学中心 耳鼻喉口腔颌面外科, 上海 200127
  • 出版日期:2022-01-10 发布日期:2022-02-22
  • 通讯作者: 陈洁. E-mail:13611715123@163.com
  • 基金资助:
    国家自然科学基金资助项目(81700907);上海交通大学医学院附属上海儿童医学中心“3311”项目(ZCQ-SCMC2018-9);上海市综合医院中西医结合专项(ZHYY-ZXYJHZX-202009)

Research progress on auditory risk factors and hearing screening methods among neonates

PAN Linlin, KONG Lingyi,ZHAI Feng, CHEN Jie   

  1. Department of Otolaryngology and Oral & Maxillofacial Surgery, Shanghai Children's Medical Center Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200127, China
  • Online:2022-01-10 Published:2022-02-22

摘要: 听力障碍严重影响新生儿言语和识字能力发育,阻碍儿童社交、认知和学习。影响新生儿听力的因素众多,发病机制和特点各异。新生儿的听力障碍非遗传因素主要包括早产、低出生体质量、新生儿高胆红素血症、新生儿缺氧、感染、耳毒性药物用药史等;遗传因素主要包括GJB2、GJB3、SLC26A4和线粒体基因MT-RNR1变异。耳声发射、自动听觉脑干反应和声导抗检查的联合应用可有效提高新生儿听力障碍筛查的准确率,有助于早期诊断和干预。

关键词: 听力障碍, 新生儿, 听力筛查, 耳声发射, 自动听觉脑干反应, 声导抗

Abstract: Newborn hearing loss results in not only delayed language and speech development but also poor social, recognitional, and educational performance. Several factors have an impact on neonatal hearing. However, the pathogenesis and characteristics of the factors vary based on the type of factor contributing to hearing impairment in neonates. Non-genetic factors mainly include preterm birth, low birth weight, neonatal hyperbilirubinemia, newborn hypoxia, infection, and ototoxic medication, whereas genetic factors mainly include GJB2, GJB3, SLC26A4, and mitochondrially encoded MT-RNR1 variation. Combined application of otoacoustic emission, automatic auditory brainstem response, and acoustic immittance test can effectively improve the accuracy of neonatal hearing impairment screening, which is helpful for early diagnosis and intervention.

Key words: Hearing loss, Neonates, Hearing screening, Otoacoustic emission, Automated auditory brainstem response, Acoustic immittance

中图分类号: 

  • R764.5
[1] Newborn and infant hearing screening: current issues and guiding principles for action[R]. Geneva, Switzerland: WHO, 2010.
[2] Yun CF, Wang ZJ, Gao JM, et al. Prevalence and social risk factors for hearing impairment in Chinese children-A national survey[J]. Int J Environ Res Public Health, 2017, 14(1): E88. doi:10.3390/ijerph14010088.
[3] van der Straaten TFK, Rieffe C, Soede W, et al. Quality of life of children with hearing loss in special and mainstream education: a longitudinal study[J]. Int J Pediatr Otorhinolaryngol, 2020, 128: 109701. doi:10.1016/j.ijporl.2019.109701.
[4] Wilson BS, Tucci DL, Merson MH, et al. Global hearing health care: new findings and perspectives[J]. Lancet, 2017, 390(10111): 2503-2515. doi:10.1016/S0140-6736(17)31073-5.
[5] The Joint Committee on Infant Hearing. Year 2019 position statement: principles and guidelines for early hearing detection and intervention programs[J]. Journal of Early Hearing Detection and Intervention, 2019, 4(2): 1-44. doi: 10.15142/fptk-b748.
[6] American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs[J]. Pediatrics, 2007, 120(4): 898-921. doi:10.1542/peds.2007-2333.
[7] Korver AM, Smith RJ, Van Camp G, et al. Congenital hearing loss[J]. Nat Rev Dis Primers, 2017, 3: 16094. doi:10.1038/nrdp.2016.94.
[8] Casazza G, Meier JD. Evaluation and management of syndromic congenital hearing loss[J]. Curr Opin Otolaryngol Head Neck Surg, 2017, 25(5): 378-384. doi:10.1097/MOO.0000000000000397.
[9] Wroblewska-Seniuk K, Greczka G, Dabrowski P, et al. Hearing impairment in premature newborns-Analysis based on the national hearing screening database in Poland[J]. PLoS One, 2017, 12(9): e0184359. doi:10.1371/journal.pone.0184359.
[10] van Dommelen P, de Graaff-Korf K, Verkerk PH, et al. Maturation of the auditory system in normal-hearing newborns with a very or extremely premature birth[J]. Pediatr Neonatol, 2020, 61(5): 529-533. doi:10.1016/j.pedneo.2020.05.014.
[11] van Dommelen P, Verkerk PH, van Straaten HL, et al. Hearing loss by week of gestation and birth weight in very preterm neonates[J]. J Pediatr, 2015, 166(4): 840-843.e1. doi:10.1016/j.jpeds.2014.12.041.
[12] Wang C, Jiang ZD. Brainstem auditory abnormality in extremely premature babies and the impact of neonatal bronchopulmonary dysplasia[J]. Acta Obstet Gynecol Scand, 2018, 97(5): 545-551. doi:10.1111/aogs.13312.
[13] Frezza S, Catenazzi P, Gallus R, et al. Hearing loss in very preterm infants: should we wait or treat?[J]. Acta Otorhinolaryngol Italica, 2019, 39(4): 257-262. doi:10.14639/0392-100X-2116.
[14] Wang CH, Yang CY, Lien R, et al. Prevalence and independent risk factors for hearing impairment among very low birth weight infants[J]. Int J Pediatr Otorhinolaryngol, 2017, 93: 123-127. doi:10.1016/j.ijporl.2016.12.029.
[15] Martínez-Cruz CF, García Alonso-Themann P, Poblano A, et al. Hearing loss, auditory neuropathy, and neurological co-morbidity in children with birthweight <750 G[J]. Arch Med Res, 2012, 43(6): 457-463. doi:10.1016/j.arcmed.2012.08.007.
[16] 张玲, 叶海波, 时海波. 胆红素所致听觉系统神经损害的新机制[J]. 山东大学耳鼻喉眼学报, 2019,33(3): 31-35. doi:10.6040/j.issn.1673-3770.1.2018.044. ZHANG Ling, YE Haibo, SHI Haibo. A new mechanism of bilirubin-induced auditory nervous system injury[J]. J Otolaryngol Ophthalmol Shandong Univ, 2019,33(3): 31-35. doi:10.6040/j.issn.1673-3770.1.2018.044.
[17] Olds C, Oghalai JS. Bilirubin-induced audiologic injury in preterm infants[J]. Clin Perinatol, 2016, 43(2): 313-323. doi:10.1016/j.clp.2016.01.006.
[18] Singh A, Francis HW, Smith PB, et al. Association between hyperbilirubinemia and hearing screen failure in the neonatal intensive care unit in infants born preterm[J]. J Pediatr, 2021, 231: 68-73. doi:10.1016/j.jpeds.2020.12.059.
[19] Boskabadi H, Zakerihamidi M, Moradi A, et al. Risk factors for sensorineural hearing loss in neonatal hyperbilirubinemia[J]. Iran J Otorhinolaryngol, 2018, 30(99): 195-202.
[20] Amin SB, Wang HY, Laroia N, et al. Unbound bilirubin and auditory neuropathy spectrum disorder in late preterm and term infants with severe jaundice[J]. J Pediatr, 2016, 173: 84-89. doi:10.1016/j.jpeds.2016.02.024.
[21] Amin SB, Saluja S, Saili A, et al. Auditory toxicity in late preterm and term neonates with severe jaundice[J]. Dev Med Child Neurol, 2017, 59(3): 297-303. doi:10.1111/dmcn.13284.
[22] Xu J, Weng ML, Li NQ, et al. Relationship research between auditory neuropathy spectrum disorder and exchange transfusion in neonates with severe hyperbilirubinemia[J]. Int J Pediatr Otorhinolaryngol, 2019, 123: 146-150. doi:10.1016/j.ijporl.2019.04.044.
[23] Kvestad E, Lie KK, Eskild A, et al. Sensorineural hearing loss in children: the association with Apgar score. A registry-based study of 392, 371 children in Norway[J]. Int J Pediatr Otorhinolaryngol, 2014, 78(11): 1940-1944. doi:10.1016/j.ijporl.2014.08.032.
[24] Zhai F, Fang XH, Li YB, et al. Risk factors for failure in first-time hearing screening tests among high-risk neonates in neonatal intensive care unit[J]. Audiol Neurootol, 2021: 1-8. doi:10.1159/000512761.
[25] Fitzgerald MP, Reynolds A, Garvey CM, et al. Hearing impairment and hypoxia ischaemic encephalopathy: Incidence and associated factors[J]. Eur J Paediatr Neurol, 2019, 23(1): 81-86. doi:10.1016/j.ejpn.2018.10.002.
[26] Kadıoglu ??塁im??塂ek G, Kutman HGK, Canpolat FE, et al. Hearing screening failure rate in newborn infants with hypoxic ischemic encephalopathy[J]. Int J Pediatr Otorhinolaryngol, 2020, 128: 109691. doi:10.1016/j.ijporl.2019.109691.
[27] Lin JC, Huang H, Lv G, et al. Chronic prenatal hypoxia impairs cochlear development, a mechanism involving connexin26 expression and promoter methylation[J]. Int J Mol Med, 2018, 41(2): 852-858. doi:10.3892/ijmm.2017.3303.
[28] 冯爽, 陈敬伟, 黄振云, 等. 缺氧对耳蜗听神经元电压门控性钠通道及凋亡因子表达的影响[J]. 现代医药卫生, 2019, 35(11): 1616-1618. doi:10.3969/j.issn.1009-5519.2019.11.005. FENG Shuang, CHEN Jingwei, HUANG Zhenyun, et al. Regulation on voltage gated sodium channels and Caspase-3 expression in spiral ganglion neurons by hypoxia[J]. J Mod Med Heal, 2019, 35(11): 1616-1618. doi:10.3969/j.issn.1009-5519.2019.11.005.
[29] Leite JN, Silva VS, Buzo BC. Emissões otoacústicas em recém-nascidos com hipóxia perinatal leve e moderada[J]. CoDAS, 2016, 28(2): 93-98. doi:10.1590/2317-1782/20162015086.
[30] Jiang ZD, Zang Z, Wilkinson AR. Cochlear function in 1-year-old term infants born with hypoxia-ischaemia or low Apgar scores[J]. J Paediatr Child Heal, 2012, 48(2): 160-165. doi:10.1111/j.1440-1754.2011.02066.x.
[31] Ribeiro GE, Silva DP, Montovani JC. Transient evoked otoacoustic emissions and auditory brainstem response in infants with perinatal asphyxia[J]. Int J Pediatr Otorhinolaryngol, 2016, 89: 136-139. doi:10.1016/j.ijporl.2016.08.009.
[32] 王鸿南, 王希军, 宋江顺. 急性缺氧对豚鼠听性脑干反应的影响[J]. 第一军医大学学报, 2000,20(3): 247-249. WANG Hongnan, WANG Xijun, SONG Jiangshun. The effects of acute Anoxia on the auditory brainstem response of Guinea pigs[J]. J First Mil Med Univ, 2000,20(3): 247-249.
[33] Jiang ZD, Shao XM, Wilkinson AR. Brainstem auditory-evoked responses in full-term newborn infants with temporary low Apgar score[J]. Acta Otolaryngol, 2005, 125(2): 163-168. doi:10.1080/00016480410017684.
[34] Michniewicz B, Wroblewska-Seniuk K, Amara JA, et al. Hearing impairment in infants with hypoxic ischemic encephalopathy treated with hypothermia[J]. Ther Hypothermia Temp Manag, 2021: ther.2020.0043. doi:10.1089/ther.2020.0043.
[35] Khairy MA, Abuelhamed WA, Ahmed RS, et al. Hearing loss among high-risk newborns admitted to a tertiary Neonatal Intensive Care Unit[J]. J Matern Fetal Neonatal Med, 2018, 31(13): 1756-1761. doi:10.1080/14767058.2017.1326902.
[36] Leung JC, Cifra CL, Agthe AG, et al. Antenatal factors modulate hearing screen failure risk in preterm infants[J]. Arch Dis Child Fetal Neonatal Ed, 2016, 101(1): F56-F61. doi:10.1136/archdischild-2014-307843.
[37] Helmstaedter V, Buechner A, Stolle S, et al. Cochlear implantation in children with meningitis related deafness: The influence of electrode impedance and implant charge on auditory performance - A case control study[J]. Int J Pediatr Otorhinolaryngol, 2018, 113: 102-109. doi:10.1016/j.ijporl.2018.07.034.
[38] Leruez-Ville M, Foulon I, Pass R, et al. Cytomegalovirus infection during pregnancy: state of the science[J]. Am J Obstet Gynecol, 2020, 223(3): 330-349. doi:10.1016/j.ajog.2020.02.018.
[39] Demmler-Harrison GJ, Miller JA, Houston Congenital Cytomegalovirus Longitudinal Study Group. Maternal Cytomegalovirus immune status and hearing loss outcomes in congenital Cytomegalovirus-infected offspring[J]. PLoS One, 2020, 15(10): e0240172. doi:10.1371/journal.pone.0240172.
[40] Goderis J, Keymeulen A, Smets K, et al. Hearing in children with congenital Cytomegalovirus infection: results of a longitudinal study[J]. J Pediatr, 2016, 172: 110-115.e2. doi:10.1016/j.jpeds.2016.01.024.
[41] Congenital Cytomegalovirus infection: update on treatment[J]. BJOG: Int J Obstet Gy, 2018, 125(1): e1-e11. doi:10.1111/1471-0528.14836.
[42] Whitley RJ. Congenital Cytomegalovirus and neonatal Herpes simplex virus infections: to treat or not to treat?[J]. Pediatr Infect Dis J, 2019, 38(6S Suppl 1): S60-S63. doi:10.1097/INF.0000000000002325.
[43] Rasmussen SA, Jamieson DJ, Honein MA, et al. Zika virus and birth defects: reviewing the evidence for causality[J]. N Engl J Med, 2016, 374(20): 1981-1987. doi:10.1056/NEJMsr1604338.
[44] Gazeta RE, Bertozzi APAP, de Cássia de Aguirre Bernardes Dezena R, et al. Three-year clinical follow-up of children intrauterine exposed to zika virus[J]. Viruses, 2021, 13(3): 523. doi:10.3390/v13030523.
[45] Leal MC, Muniz LF, Ferreira TS, et al. Hearing loss in infants with microcephaly and evidence of congenital zika virus infection-Brazil, November 2015-may 2016[J]. MMWR Morb Mortal Wkly Rep, 2016, 65(34): 917-919. doi:10.15585/mmwr.mm6534e3.
[46] Adebanjo T, Godfred-Cato S, Viens L, et al. Update: interim guidance for the diagnosis, evaluation, and management of infants with possible congenital zika virus infection - United States, October 2017[J]. MMWR Morb Mortal Wkly Rep, 2017, 66(41): 1089-1099. doi:10.15585/mmwr.mm6641a1.
[47] Huth ME, Han KH, Sotoudeh K, et al. Designer aminoglycosides prevent cochlear hair cell loss and hearing loss[J]. J Clin Invest, 2015, 125(2): 583-592. doi:10.1172/JCI77424.
[48] Koo JW, Quintanilla-Dieck L, Jiang MY, et al. Endotoxemia-mediated inflammation potentiates aminoglycoside-induced ototoxicity[J]. Sci Transl Med, 2015, 7(298): 298ra118. doi:10.1126/scitranslmed.aac5546.
[49] Barbarino JM, McGregor TL, Altman RB, et al. PharmGKB summary: very important pharmacogene information for MT-RNR1[J]. Pharmacogenet Genomics, 2016, 26(12): 558-567. doi:10.1097/FPC.0000000000000247.
[50] Yang HY, Luo HY, Zhang GW, et al. A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns[J]. BMC Med Genomics, 2021, 14(1): 61. doi:10.1186/s12920-021-00906-1.
[51] Rabiço-Costa D, Gil-da-Costa MJ, Barbosa JP, et al. Platinum-drugs ototoxicity in pediatric patients with brain tumors: a 10-year review[J]. J Pediatr Hematol Oncol, 2020, 42(1): e25-e31. doi:10.1097/MPH.0000000000001637.
[52] Wang LA, Smith PB, Laughon M, et al. Prolonged furosemide exposure and risk of abnormal newborn hearing screen in premature infants[J]. Early Hum Dev, 2018, 125: 26-30. doi:10.1016/j.earlhumdev.2018.08.009.
[53] Judge PD, Jorgensen E, Lopez-Vazquez M, et al. Medical referral patterns and etiologies for children with mild-to-severe hearing loss[J]. Ear Hear, 2019, 40(4): 1001-1008. doi:10.1097/AUD.0000000000000682.
[54] Seror J, Amand G, Guibourdenche J, et al. Anti-TPO antibodies diffusion through the placental barrier during pregnancy[J]. PLoS One, 2014, 9(1): e84647. doi:10.1371/journal.pone.0084647.
[55] Meyerhoff WL. Hypothyroidism and the ear: electrophysiological, morphological, and chemical considerations[J]. Laryngoscope, 1979, 89(10 Pt 2 Suppl 19): 1-25. doi:10.1002/lary.5540891501.
[56] Lee JA, Mehta CH, Nguyen SA, et al. Hearing outcomes in children of diabetic pregnancies[J]. Int J Pediatr Otorhinolaryngol, 2020, 132: 109925. doi:10.1016/j.ijporl.2020.109925.
[57] Bakhshaee M, Boskabadi H, Hassanzadeh M, et al. Hearing impairment in the neonate of preeclamptic women[J]. Otolaryngol Head Neck Surg, 2008, 139(6): 846-849. doi:10.1016/j.otohns.2008.09.018.
[58] Wilunda C, Yoshida S, Tanaka S, et al. Exposure to tobacco smoke prenatally and during infancy and risk of hearing impairment among children in Japan: a retrospective cohort study[J]. Paediatr Perinat Epidemiol, 2018, 32(5): 430-438. doi:10.1111/ppe.12477.
[59] Zhao HB. Hypothesis of k+-recycling defect is not a primary deafness mechanism for Cx26(GJB2)deficiency[J]. Front Mol Neurosci, 2017, 10: 162. doi:10.3389/fnmol.2017.00162.
[60] Zhu Y, Chen J, Liang C, et al. Connexin26(GJB2)deficiency reduces active cochlear amplification leading to late-onset hearing loss[J]. Neuroscience, 2015, 284: 719-729. doi:10.1016/j.neuroscience.2014.10.061.
[61] Huang SS, Huang BQ, Wang GJ, et al. The relationship between the p.V37I mutation in GJB2 and hearing phenotypes in Chinese individuals[J]. PLoS One, 2015, 10(6): e0129662. doi:10.1371/journal.pone.0129662.
[62] Morton CC, Nance WE. Newborn hearing screening: a silent revolution[J]. N Engl J Med, 2006, 354(20): 2151-2164. doi:10.1056/NEJMra050700.
[63] Wang QJ, Xiang JL, Sun J, et al. Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China[J]. Genet Med, 2019, 21(10): 2231-2238. doi:10.1038/s41436-019-0481-6.
[64] Huang SS, Huang BQ, Wang GJ, et al. The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population[J]. Int J Pediatr Otorhinolaryngol, 2017, 102: 67-70. doi:10.1016/j.ijporl.2017.09.001.
[65] Kim SY, Choi BY, Jung EY, et al. Risk factors for failure in the newborn hearing screen test in very preterm twins[J]. Pediatr Neonatol, 2018, 59(6): 586-594. doi:10.1016/j.pedneo.2018.01.014.
[66] Sasireka BI, Jaya V, Vignesh SS, et al. Clinical experience on hearing screening in twins and triplets: a retrospective study[J]. Indian J Otolaryngol Head Neck Surg, 2019, 71(3): 401-405. doi:10.1007/s12070-017-1117-2.
[67] 国家卫生和计划生育委员会新生儿疾病筛查听力诊断治疗组. 婴幼儿听力损失诊断与干预指南[J]. 中华耳鼻咽喉头颈外科杂志, 2018, 53(3): 181-188. doi:10.3760/cma.j.issn.1673-0860.2018.03.004.
[68] Kei J, Allison-Levick J, Dockray J, et al. High-frequency(1000 Hz)tympanometry in normal neonates[J]. J Am Acad Audiol, 2003, 14(1): 20-28. doi:10.3766/jaaa.14.1.4.
[69] Myers J, Kei J, Aithal S, et al. Development of a diagnostic prediction model for conductive conditions in neonates using wideband acoustic immittance[J]. Ear Hear, 2018, 39(6): 1116-1135. doi:10.1097/AUD.0000000000000565.
[70] Guo L, Xiang JL, Sun L, et al. Concurrent hearing and genetic screening in a general newborn population[J]. Hum Genet, 2020, 139(4): 521-530. doi:10.1007/s00439-020-02118-6.
[1] 陈铭,柯冰冰,崔雅琦,吴翠萍,陈正侬,李春燕,殷善开. NAD+对顺铂所致毛细胞氧化应激损伤的拮抗作用及相关基因表达调控[J]. 山东大学耳鼻喉眼学报, 2025, 39(3): 11-18.
[2] 陈丹萍,何子键,虞幼军,周晓娓. 儿童突发性聋10年住院病例的疗效及预后相关因素分析[J]. 山东大学耳鼻喉眼学报, 2025, 39(1): 16-22.
[3] 张晓,刘海红,刘薇,李颖,陈敏,刘冰,白杰,张杰,郑军,杨扬. 先天性单侧聋患儿112例临床资料分析[J]. 山东大学耳鼻喉眼学报, 2024, 38(4): 96-196.
[4] 索安奇,孙聚兴,牛红燕,周艳秋,牛鹏昊,毛文伟,李晓瑜,杨欣欣. 耳部钢筋复杂穿刺伤救治1例并文献复习[J]. 山东大学耳鼻喉眼学报, 2024, 38(2): 79-83.
[5] 熊彬彬,卢子昂,杨晶,徐文强,周潞茹,孙平原,袁丁,朱佳浩. 纯音听阈值正常的中青年耳鸣群体耳蜗功能分析[J]. 山东大学耳鼻喉眼学报, 2023, 37(4): 62-67.
[6] 李为,赵毅,葛玥铭,付洪涛,王进东,张晓龙,董洁,程钰翔. 双卵双胎和单卵双胎新生儿听力筛查结果分析[J]. 山东大学耳鼻喉眼学报, 2023, 37(2): 1-6.
[7] 吕萍,李丹丹,宋伟,洪流. 鼻内镜辅助下鼻泪道再通术治疗新生儿期泪囊炎[J]. 山东大学耳鼻喉眼学报, 2023, 37(2): 71-74.
[8] 段新艳,宋忠义,王宁,訾希存, 潘新良. DPOAE与高刺激率ABR在听力正常耳鸣患者中的应用价值[J]. 山东大学耳鼻喉眼学报, 2022, 36(5): 6-10.
[9] 朱晶,张睿,赵媛,李炀,赵昱. 新生儿咽旁间隙卡梅现象1例并文献复习[J]. 山东大学耳鼻喉眼学报, 2022, 36(4): 55-59.
[10] 盘琳琳, 方旭华, 翟丰, 桂一丁, 边洲亮, 陈洁. 新生儿动脉血血气分析与听力筛查结果相关性[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 20-24.
[11] 倪坤, 孙世冰, 李晓艳. 1 000 Hz声导抗在高危新生儿听力筛查中的应用[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 43-47.
[12] 张丰珍,王桂香,赵靖,王华,段清川,李宏彬,黑明燕,翁景文,张杰. 新生儿双侧声带麻痹临床特点及预后分析[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 86-90.
[13] 曾斌, 吕丹, 任佳, 胡娟娟, 于凌昱, 卢欢, 杨慧. 喉显微外科技术在严重新生儿上气道梗阻中的应用[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 95-99.
[14] 李元超,吴玮,王刚,屈昌北,王磊,芦文俊,李丹,韩浩伦,刘钢. 模拟失重及飞船内稳态噪声对大鼠听功能的影响[J]. 山东大学耳鼻喉眼学报, 2021, 35(5): 11-16.
[15] 杨红,滕以书,李兰,潘宏光,梁振江,韩赛红. 新生儿梨状窝瘘3例并文献复习[J]. 山东大学耳鼻喉眼学报, 2021, 35(4): 40-44.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!