Is hearing loss a feature of Joubert syndrome, a ciliopathy?

被引:11
作者
Kroes, Hester Y. [1 ]
Van Zanten, Bert G. A. [2 ]
De Ru, Sander A. [3 ]
Boon, Maartje [4 ]
Mancini, Grazia M. S. [5 ]
Van der Knaap, Marjo S. [6 ]
Poll-The, Bwee Tien [7 ]
Lindhout, Dick [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Med Genet, NL-3584 EA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Otorhinolaryngol, Rudolf Magnus Inst Neurosci, NL-3584 EA Utrecht, Netherlands
[3] Cent Mil Hosp, Dept Otorhinolaryngol, Utrecht, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Child Neurol, Groningen, Netherlands
[5] Erasmus MC, Dept Med Genet, Rotterdam, Netherlands
[6] VU Univ Med Ctr Amsterdam, Dept Child Neurol, Amsterdam, Netherlands
[7] Acad Med Ctr Amsterdam, Dept Child Neurol, Amsterdam, Netherlands
关键词
Joubert syndrome; Kinocilium; Ciliopathies; Hearing loss; Alstrom syndrome; Bardet-Biedl syndrome; Hyperacusis; ALSTROM-SYNDROME; BARDET-BIEDL; INNER-EAR; FOLLOW-UP; MUTATIONS; KINOCILIUM; INPP5E; CELLS;
D O I
10.1016/j.ijporl.2010.05.034
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective To assess if hearing loss is a feature of Joubert syndrome (JBS). one of the ciliopathies and therefore possibly associated with hearing loss Design: Retrospective case series. Setting University Children's Hospital Patients Dutch patients with JBS. Main outcome measures Audiological data. Results: Data from 22 Dutch Joubert syndrome (JBS) cases (17 males, 5 females) aged 3-40 years were available. Audiological tests were successfully performed in 14 cases Three cases (aged 17-26 years) showed very mild sensorineural hearing loss (SNHL) at different frequencies. Conductive hearing loss due to middle ear infections occurred frequently in young JBS children (6 out of 22 cases) In three cases (aged 3-13 years) the parents reported the child was hypersensitive to sound. Conclusion We found no evidence for significant hearing loss in Joubert syndrome patients. However, given the compromised speech development in JBS, conductive hearing loss due to middle ear infections should be treated vigorously SNHL at a later age cannot be excluded on the basis of our data, given the sample size Three of the older cases showed discretely Increased hearing thresholds Analogous to the ciliopathy Bardet-Biedl syndrome, where hearing thresholds were reported to be subclinically increased in a group of adolescents patients, we recommend follow-up of JBS patients in view of the possibility of progressive, late-onset SNHL. (C) 2010 Elsevier Ireland Ltd. All rights reserved
引用
收藏
页码:1034 / 1038
页数:5
相关论文
共 26 条
[1]   History of Joubert syndrome and a 30-year follow-up of the original proband [J].
Andermann, F ;
Andermann, E ;
Ptito, A ;
Fontaine, S ;
Joubert, M .
JOURNAL OF CHILD NEUROLOGY, 1999, 14 (09) :565-569
[2]   Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome [J].
Arts, Heleen H. ;
Doherty, Dan ;
van Beersum, Sylvia E. C. ;
Parisi, Melissa A. ;
Letteboer, Stef J. F. ;
Gorden, Nicholas T. ;
Peters, Theo A. ;
Maerker, Tina ;
Voesenek, Krysta ;
Kartono, Aileen ;
Ozyurek, Hamit ;
Farin, Federico M. ;
Kroes, Hester Y. ;
Wolfrum, Uwe ;
Brunner, Han G. ;
Cremers, Frans P. M. ;
Glass, Ian A. ;
Knoers, Nine V. A. M. ;
Roepman, Ronald .
NATURE GENETICS, 2007, 39 (07) :882-888
[3]   Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies [J].
Bielas, Stephanie L. ;
Silhavy, Jennifer L. ;
Brancati, Francesco ;
Kisseleva, Marina V. ;
Al-Gazali, Lihadh ;
Laszlo Sztriha ;
Bayoumi, Riad A. ;
Zaki, Maha S. ;
Abdel-Aleem, Alice ;
Rosti, Rasim Ozgur ;
Kayserili, Hulya ;
Swistun, Dominika ;
Scott, Lesley C. ;
Bertini, Enrico ;
Boltshauser, Eugen ;
Fazzi, Elisa ;
Travaglini, Lorena ;
Field, Seth J. ;
Gayral, Stephanie ;
Jacoby, Monique ;
Schurmans, Stephane ;
Dallapiccola, Bruno ;
Majerus, Philip W. ;
Valente, Enza Maria ;
Gleeson, Joseph G. .
NATURE GENETICS, 2009, 41 (09) :1032-U108
[4]   DEAFNESS AND THE LAURENCE-MOON-BIEDL SYNDROME [J].
BURN, RA .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1950, 34 (02) :65-88
[5]   Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome [J].
Cantagrel, Vincent ;
Silhavy, Jennifer L. ;
Bielas, Stephanie L. ;
Swistun, Dominika ;
Marsh, Sarah E. ;
Bertrand, Julien Y. ;
Audollent, Sophie ;
Attie-Bitach, Tania ;
Holden, Kenton R. ;
Dobyns, William B. ;
Traver, David ;
Al-Gazali, Lihadh ;
Ali, Bassam R. ;
Lindner, Tom H. ;
Caspary, Tamara ;
Otto, Edgar A. ;
Hildebrandt, Friedhelm ;
Glass, Ian A. ;
Logan, Clare V. ;
Johnson, Colin A. ;
Bennett, Christopher ;
Brancati, Francesco ;
Valente, Enza Maria ;
Woods, C. Geoffrey ;
Gleeson, Joseph G. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 83 (02) :170-179
[6]   OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin [J].
Coene, Karlien L. M. ;
Roepman, Ronald ;
Doherty, Dan ;
Afroze, Bushra ;
Kroes, Hester Y. ;
Letteboer, Stef J. F. ;
Ngu, Lock H. ;
Budny, Bartlomiej ;
van Wijk, Erwin ;
Gorden, Nicholas T. ;
Azhimi, Malika ;
Thauvin-Robinet, Christel ;
Veltman, Joris A. ;
Boink, Mireille ;
Kleefstra, Tjitske ;
Cremers, Frans P. M. ;
van Bokhoven, Hans ;
de Brouwer, Arjan P. M. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 85 (04) :465-481
[7]   Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome [J].
Collin, GB ;
Marshall, JD ;
Ikeda, A ;
So, WV ;
Russell-Eggitt, I ;
Maffei, P ;
Beck, S ;
Boerkoel, CF ;
Sicolo, N ;
Martin, M ;
Nishina, PM ;
Naggert, JK .
NATURE GENETICS, 2002, 31 (01) :74-78
[8]   Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation [J].
Edvardson, Simon ;
Shaag, Avraham ;
Zenvirt, Shamir ;
Erlich, Yaniv ;
Hannon, Gregory J. ;
Shanske, Alan L. ;
Gomori, John Moshe ;
Ekstein, Joseph ;
Elpeleg, Orly .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (01) :93-97
[9]   ULTRASTRUCTURE OF KINOCILIUM OF SENSORY CELLS IN INNER EAR AND LATERAL LINE ORGANS [J].
FLOCK, A ;
DUVALL, AJ .
JOURNAL OF CELL BIOLOGY, 1965, 25 (1P1) :1-+
[10]   The molecular architecture of the inner ear [J].
Forge, A ;
Wright, T .
BRITISH MEDICAL BULLETIN, 2002, 63 :5-24