Cochlear implantation in children with auditory neuropathy: Lessons from Brown-Vialetto-Van Laere syndrome

被引:21
作者
Anderson, Phoebe [1 ]
Schaefer, Simone [2 ]
Henderson, Lise [3 ]
Bruce, Iain A. [2 ,4 ]
机构
[1] Univ Manchester, Manchester Med Sch, Manchester, Lancs, England
[2] Manchester Univ NHS Fdn Trust, Royal Manchester Childrens Hosp, Manchester Acad Hlth Sci Ctr, Paediat ENT Dept, Ward 79,Oxford Rd, Manchester M13 9WL, Lancs, England
[3] Manchester Univ NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Richard Ramsden Ctr Auditory Implants, Manchester, Lancs, England
[4] Univ Manchester, Fac Biol Med & Hlth, Div Infect Immun & Resp Med, Manchester, Lancs, England
关键词
Cochlear implantation; Auditory neuropathy; Brown-Vialetto-Van Laere syndrome; Riboflavin transporter deficiency; Outcomes; Retrospective study; Auditory perception; Parental benefit; BULBAR PALSY; MUTATIONS; DEAFNESS; AGE;
D O I
10.1080/14670100.2018.1534035
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Brown-Vialetto-Van Laere syndrome (BVVL) is a rare neurodegenerative disorder associated with auditory neuropathy (AN). The decision process for CI in AN is evolving with increasing evidence of efficacy. We evaluated the benefit of CI in children with BVVL syndrome. Methods: A retrospective study reviewed the pre- and post-operative hearing outcomes of three patients with BVVL who presented for CI. A fourth patient with BVVL who was not suitable for CI is also discussed. The primary outcomes were hearing thresholds and auditory perception. Outcome measurement instruments included visual reinforcement audiometry (VRA) or Play Audiometry (PA), Categories of Auditory Performance (CAP) and Auditory Speech Sound Evaluation (ASSE). Secondary outcomes were parental report (BAPP questionnaire), the perception of our SaLT and compliance. Results: Patient 1 had ASSE levels of 40-45 dB HL 1 year post-operatively, and CAP score had improved from 2 to 5. At 2-year review, aided thresholds were 40 dB at 2-4 kHz. Three months following CI, the CAP score of Patient 2 had improved from 3 to 5. At 6 months, thresholds were 25-30 dB at 2-4 kHz. Single words/phrases are used by both patients and benefit is reported by both families. Patient 3 has recently undergone CI, having been previously rejected at another centre. Three months following CI, his thresholds were 35-40 dB at 2-4 kHz and increased use of sign and vocalization is reported. Conclusion: CI in children with AN complicating BVVL has a variable, but a positive effect. Other manifestations of BVVL make measuring benefit challenging, in the absence of a 'bespoke' measurement instrument for children with complex needs. This study provides further evidence for the benefit of CI in children with AN.
引用
收藏
页码:31 / 38
页数:8
相关论文
共 24 条
[1]   The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives [J].
Bosch, Annet M. ;
Stroek, Kevin ;
Abeling, Nico G. ;
Waterham, Hans R. ;
Ijlst, Lodewijk ;
Wanders, Ronald J. A. .
ORPHANET JOURNAL OF RARE DISEASES, 2012, 7
[2]  
Brown C.H., 1894, J Nerv Ment Dis, V19, P707, DOI DOI 10.1097/00005053-189411000-00003
[3]   Auditory neuropathy spectrum disorder with Brown-Vialetto-Van Laere syndrome: challenges in hearing rehabilitation [J].
Chandran, R. ;
Alexander, M. ;
Naina, P. ;
Balraj, A. .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2015, 129 (05) :504-508
[4]   Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 [J].
Foley, A. Reghan ;
Menezes, Manoj P. ;
Pandraud, Amelie ;
Gonzalez, Michael A. ;
Al-Odaib, Ahmad ;
Abrams, Alexander J. ;
Sugano, Kumiko ;
Yonezawa, Atsushi ;
Manzur, Adnan Y. ;
Burns, Joshua ;
Hughes, Imelda ;
McCullagh, B. Gary ;
Jungbluth, Heinz ;
Lim, Ming J. ;
Lin, Jean-Pierre ;
Megarbane, Andre ;
Urtizberea, J. Andoni ;
Shah, Ayaz H. ;
Antony, Jayne ;
Webster, Richard ;
Broomfield, Alexander ;
Ng, Joanne ;
Mathew, Ann A. ;
O'Byrne, James J. ;
Forman, Eva ;
Scoto, Mariacristina ;
Prasad, Manish ;
O'Brien, Katherine ;
Olpin, Simon ;
Oppenheim, Marcus ;
Hargreaves, Iain ;
Land, John M. ;
Wang, Min X. ;
Carpenter, Kevin ;
Horvath, Rita ;
Straub, Volker ;
Lek, Monkol ;
Gold, Wendy ;
Farrell, Michael O. ;
Brandner, Sebastian ;
Phadke, Rahul ;
Matsubara, Kazuo ;
McGarvey, Michael L. ;
Scherer, Steven S. ;
Baxter, Peter S. ;
King, Mary D. ;
Clayton, Peter ;
Rahman, Shamima ;
Reilly, Mary M. ;
Ouvrier, Robert A. .
BRAIN, 2014, 137 :44-56
[5]   BROWN-VIALETTO-VANLAERE SYNDROME [J].
FRANCIS, DA ;
PONSFORD, JR ;
WILES, CM ;
THOMAS, PK ;
DUCHEN, LW .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1993, 19 (01) :91-94
[6]   PONTO-BULBAR PALSY WITH DEAFNESS (BROWN-VIALETTO-VANLAERE SYNDROME) - A REPORT ON 3 CASES [J].
GALLAI, V ;
HOCKADAY, JM ;
HUGHES, JT ;
LANE, DJ ;
OPPENHEIMER, DR ;
RUSHWORTH, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1981, 50 (02) :259-275
[7]   Auditory neuropathies: understanding their pathogenesis to illuminate intervention strategies [J].
Giraudet, Fabrice ;
Avan, Paul .
CURRENT OPINION IN NEUROLOGY, 2012, 25 (01) :50-56
[8]   Brown-Vialetto-Van Laere Syndrome, a Ponto-Bulbar Palsy with Deafness, Is Caused by Mutations in C20orf54 [J].
Green, Peter ;
Wiseman, Matthew ;
Crow, Yanick J. ;
Houlden, Henry ;
Riphagen, Shelley ;
Lin, Jean-Pierre ;
Raymond, F. Lucy ;
Childs, Anne-Marie ;
Sheridan, Eamonn ;
Edwards, Sian ;
Josifova, Dragana J. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (03) :485-489
[9]   Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome [J].
Haack, Tobias B. ;
Makowski, Christine ;
Yao, Yoshiaki ;
Graf, Elisabeth ;
Hempel, Maja ;
Wieland, Thomas ;
Tauer, Ulrike ;
Ahting, Uwe ;
Mayr, Johannes A. ;
Freisinger, Peter ;
Yoshimatsu, Hiroki ;
Inui, Ken ;
Strom, Tim M. ;
Meitinger, Thomas ;
Yonezawa, Atsushi ;
Prokisch, Holger .
JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 (06) :943-948
[10]   Maternal Riboflavin Deficiency, Resulting in Transient Neonatal-Onset Glutaric Aciduria Type 2, Is Caused by a Microdeletion in the Riboflavin Transporter Gene GPR172B [J].
Ho, Gladys ;
Yonezawa, Atsushi ;
Masuda, Satohiro ;
Inui, Ken-ichi ;
Sim, Keow G. ;
Carpenter, Kevin ;
Olsen, Rikke K. J. ;
Mitchell, John J. ;
Rhead, William J. ;
Peters, Gregory ;
Christodoulou, John .
HUMAN MUTATION, 2011, 32 (01) :E1976-E1984