Literature DB >> 27779564

X-linked Malformation and Cochlear Implantation.

Henrik Smeds1, Jeremy Wales, Filip Asp, Ulrika Löfkvist, Babak Falahat, Britt-Marie Anderlid, Lena Anmyr, Eva Karltorp.   

Abstract

OBJECTIVE: To evaluate if cochlear implantation is safe and constitutes an option for hearing rehabilitation of children with x-linked inner ear malformation. STUDY
DESIGN: Retrospective patient review in combination with a multidisciplinary follow-up.
SETTING: Tertiary referral hospital and cochlear implant program. PATIENTS: Ten children with severe-profound mixed hearing loss and radiological findings consistent with Incomplete Partition type 3 cochlear malformation received cochlear implants during the years 2007 to 2015. Nine of the children had a mutation affecting the gene POU3F4 on Xq21. INTERVENTION: Cochlear implantation. MAIN OUTCOME MEASURES: Surgical events, intraoperative measures and electrical stimulation levels, hearing and spoken language abilities.
RESULTS: In all, 15 cochlear implantations were performed. In three cases the electrode was found to be in the internal auditory canal on intraoperative x-ray and repositioned successfully. One child had a postoperative rhinorrhea confirmed to be cerebrospinal fluid but this resolved on conservative treatment. No severe complications occurred. Postoperative electrical stimulation levels were higher in 9 of 10 children, as compared with typically reported average levels in patients with a normal cochlea. Eight patients developed spoken language to various degrees while two were still at precommunication level. However, speech recognition scores were lower than average pediatric cases.
CONCLUSION: Cochlear implantation is a safe procedure for children with severe-profound mixed hearing loss related to POU3F4 mutation inner ear malformation. The children develop hearing and spoken language but outcome is below average for pediatric CI recipients.

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Year:  2017        PMID: 27779564     DOI: 10.1097/MAO.0000000000001253

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  8 in total

1.  [Incomplete partition type III revisited-long-term results following cochlear implant. German version].

Authors:  A Alballaa; A Aschendorff; S Arndt; T Hildenbrand; C Becker; F Hassepass; R Laszig; R Beck; I Speck; T Wesarg; M C Ketterer
Journal:  HNO       Date:  2019-10       Impact factor: 1.284

2.  Incomplete partition type III revisited-long-term results following cochlear implant.

Authors:  A Alballaa; A Aschendorff; S Arndt; T Hildenbrand; C Becker; F Hassepass; R Laszig; R Beck; I Speck; T Wesarg; M C Ketterer
Journal:  HNO       Date:  2020-01       Impact factor: 1.284

3.  A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.

Authors:  Ahmet M Tekin; Marco Matulic; Wim Wuyts; Masoud Zoka Assadi; Griet Mertens; Vincent van Rompaey; Yongxin Li; Paul van de Heyning; Vedat Topsakal
Journal:  Genes (Basel)       Date:  2021-04-21       Impact factor: 4.096

Review 4.  X-Linked Sensorineural Hearing Loss: A Literature Review.

Authors:  Virginia Corvino; Pasqualina Apisa; Rita Malesci; Carla Laria; Gennaro Auletta; Annamaria Franzé
Journal:  Curr Genomics       Date:  2018-08       Impact factor: 2.236

5.  Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III.

Authors:  Ying Chen; Jiajun Qiu; Yingwei Wu; Huan Jia; Yi Jiang; Mengda Jiang; Zhili Wang; Hai-Bin Sheng; Lingxiang Hu; Zhihua Zhang; Zhaoyan Wang; Yun Li; Zhiwu Huang; Hao Wu
Journal:  Orphanet J Rare Dis       Date:  2022-02-21       Impact factor: 4.123

6.  Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation.

Authors:  Xiuhua Chao; Yun Xiao; Fengguo Zhang; Jianfen Luo; Ruijie Wang; Wenwen Liu; Haibo Wang; Lei Xu
Journal:  Neural Plast       Date:  2020-09-01       Impact factor: 3.599

7.  A novel POU domain class 3 transcription factor 4 mutation causes X-linked non-syndromic hearing loss in a Chinese family.

Authors:  Hong-Min Wu; Hui-Qun Jie; Hui Wang; Ya-Qin Wu; Zheng-Nong Chen; Ya-Zhi Xing; Ji-Ping Wang; Hai-Bo Shi; Shan-Kai Yin
Journal:  Chin Med J (Engl)       Date:  2019-09-20       Impact factor: 2.628

8.  X-linked Malformation Deafness: Neurodevelopmental Symptoms Are Common in Children With IP3 Malformation and Mutation in POU3F4.

Authors:  Henrik Smeds; Jeremy Wales; Eva Karltorp; Britt-Marie Anderlid; Cecilia Henricson; Filip Asp; Lena Anmyr; Kristina Lagerstedt-Robinson; Ulrika Löfkvist
Journal:  Ear Hear       Date:  2022 Jan/Feb       Impact factor: 3.562

  8 in total

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