[1] Okumura T, Takahashi H, Honjo I, et al. Sensorineural hearing loss in patients with large vestibular aqueduct[J]. Laryngoscope, 1995, 105(3 Pt 1):289-293; discussion 293-294. [2] Kaga K. Cochlear implantation in children with inner ear malformation and cochlear nerve deficiency[M]. Singapore: Springer, 2017. [3] 倪道凤. 内耳畸形的分类[J]. 听力学及言语疾病杂志, 2019, 27(1):1-5. [4] World Health Organization. With adaptations from report of the first informal consultation on future organization development for the prevention of deafness and hearing impairment[R]. Geneva: WHO,1997. [5] Jack K, 韩德民, 莫玲燕. 临床听力学[M]. 北京: 人民卫生出版社, 2006. [6] Valvassori G E, Clemis J D. The large vestibular aqueduct syndrome[J]. Laryngoscope, 1978, 88(5):723-728. [7] Emmrich J V, Fatterpekar G M. Dilated dysplastic vestibule: a new computed tomographic finding in patients with large vestibular aqueduct syndrome[J]. J Comput Assist Tomogr, 2011, 35(6):674-678. [8] Weichbold V, Nekahm-Heis D, Welzl-Mueller K. Universal newborn hearing screening and postnatal hearing loss[J]. Pediatrics, 2006, 117(4):e631-e636. [9] Young N M, Reilly B K, Burke L. Limitations of universal newborn hearing screening in early identification of pediatric cochlear implant candidates[J]. Arch Otolaryngol Head Neck Surg, 2011, 137(3):230-234. [10] Dedhia K, Kitsko D, Sabo D N, et al. Children with sensorineural hearing loss after passing the newborn hearing screen[J]. JAMA Otolaryngol Head Neck Surg, 2013, 139(2):119-123. [11] 杨亚利, 黄丽辉, 程晓华, 等. 前庭导水管扩大患儿的发现途径与首诊年龄[J]. 临床耳鼻咽喉头颈外科杂志, 2014, 28(22):1754-1758. [12] 孙宝春, 代志瑶, 黄莎莎, 等. GJB2、SLC26A4基因致病性突变与内耳CT表型关系的研究[J]. 中华耳科学杂志, 2014, 12(1):30-33. [13] 朱庆文, 臧雯, 袁永一, 等. 内耳畸形相关SLC26A4基因的研究[J]. 临床耳鼻咽喉头颈外科杂志, 2012, 26(1):22-26. [14] Fitoz S, Sennarog∨lu L, Incesulu A, et al. SLC26A4 mutations are associated with a specific inner ear malformation[J]. Int J Pediatr Otorhinolaryngol, 2007, 71(3):479-486. |