[1] Sennarolu L, Saatci I. A new classification for cochleovestibular malformations[J]. Laryngoscope, 2002, 112(12): 2230-2241.
[2] Xue S J, Wei X M, Kong Y, et al. Trends in research on cochlear implantation with inner ear malformation: a bibliometric and visualization analysis from 1986 to 2024[J]. Eur Arch Otorhinolaryngol, 2024, 281(11): 5657-5667.
[3] Archbold S, Lutman M E, Marshall D H. Categories of auditory performance[J]. Ann Otol Rhinol Laryngol Suppl, 1995, 166: 312-314.
[4] Allen M C, Nikolopoulos T P, O'Donoghue G M. Speech intelligibility in children after cochlear implantation[J]. Am J Otol, 1998, 19(6): 742-746.
[5] Jackler R K, Luxford W M, House W F. Congenital malformations of the inner ear: a classification based on embryogenesis[J]. Laryngoscope, 1987, 97(3 Pt 2 Suppl 40): 2-14.
[6] Sennarolu L,Bajin M D. Current management of inner ear malformations[J]. Balkan Med J, 2017, 34(5): 397-411.
[7] Suk Y, Lee J H, Lee K S. Surgical outcomes after cochlear implantation in children with incomplete partition type I: comparison with deaf children with a normal inner ear structure[J]. Otol Neurotol, 2015, 36(1): e11-e17.
[8] Catli T, Uckan B, Olgun L. Speech and language development after cochlear implantation in children with bony labyrinth malformations: long-term results[J]. Eur Arch Otorhinolaryngol, 2015, 272(11):3131-3136.
[9] Sennarolu L. Histopathology of inner ear malformations: do we have enough evidence to explain pathophysiology?[J]. Cochlear Implants Int, 2016, 17(1): 3-20.
[10] Tyagi I, Syal R, Goyal A. Cerebrospinal fluid otorhinorrhoea due to inner-ear malformations: clinical presentation and new perspectives in management[J]. J Laryngol Otol, 2005, 119(9): 714-718.
[11] Isaacson B, Booth T, Kutz J W J, et al. Labyrinthitis ossificans: how accurate is MRI in predicting cochlear obstruction?[J]. Otolaryngol Head Neck Surg (1979), 2009, 140(5): 692-696.
[12] Wang B, Dai W J, Cheng X T, et al. Cerebrospinal fluid otorrhea secondary to congenital inner ear dysplasia: diagnosis and management of 18 cases[J]. J Zhejiang Univ Sci B, 2019, 20(2): 156-163.
[13] Yi H J, Guo H, Ch W, et al. Use of the translabyrinthine approach to repair congenital spontaneous cerebrospinal fluid leakage in five Chinese patients with Mondini dysplasia[J]. Int J Pediatr Otorhinolaryngol, 2013, 77(12): 1965-1968.
[14] Wang J, Li Y X, Chen S B, et al. Long-term outcomes of a transmastoid lateral semicircular canal approach to congenital CSF otorrhea in children associated with recurrent meningitis and severe inner ear malformation[J]. Int J Pediatr Otorhinolaryngol, 2016, 87: 185-189.
[15] Inscoe J R, Bones C. Additional difficulties associated with aetiologies of deafness: outcomes from a parent questionnaire of 540 children using cochlear implants[J]. Cochlear Implants Int, 2016, 17(1): 21-30.
[16] Yetiser S, Karaman K. Double challenge: cochlear implantation in the only hearing ear with progressive hearing loss following meningitis and vestibular dysfunction after implantation[J]. J Otol, 2020, 15(2): 74-76.
|