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Hearing loss in children with Fabry disease

BACKGROUND: Hearing loss (HL) is a well-known feature of Fabry disease (FD). Its presence and characteristics have mainly been studied in adult patients, while only limited data are available on the presence and degree of HL in children with FD. This prompted us to study hearing sensitivity in pedia...

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Autores principales: Suntjens, E., Dreschler, W. A., Hess-Erga, J., Skrunes, R., Wijburg, F. A., Linthorst, G. E., Tøndel, C., Biegstraaten, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579138/
https://www.ncbi.nlm.nih.gov/pubmed/28567540
http://dx.doi.org/10.1007/s10545-017-0051-5
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author Suntjens, E.
Dreschler, W. A.
Hess-Erga, J.
Skrunes, R.
Wijburg, F. A.
Linthorst, G. E.
Tøndel, C.
Biegstraaten, M.
author_facet Suntjens, E.
Dreschler, W. A.
Hess-Erga, J.
Skrunes, R.
Wijburg, F. A.
Linthorst, G. E.
Tøndel, C.
Biegstraaten, M.
author_sort Suntjens, E.
collection PubMed
description BACKGROUND: Hearing loss (HL) is a well-known feature of Fabry disease (FD). Its presence and characteristics have mainly been studied in adult patients, while only limited data are available on the presence and degree of HL in children with FD. This prompted us to study hearing sensitivity in pediatric FD patients. METHODS: All available audiograms of the Dutch and Norwegian children with FD were retrospectively collected. First, hearing sensitivity was determined by studying hearing thresholds at low, high, and ultra-high frequencies in children with FD and comparing them to zero dB HL, i.e., healthy children. In addition, the presence and type of slight/mild HL (defined as hearing thresholds at low frequencies of 25–40 dB HL) and moderate to severe HL (hearing thresholds >40 dB HL) at first visit were analyzed. If available, follow-up data were used to estimate the natural course of hearing sensitivity and HL in children with FD. RESULTS: One-hundred-thirteen audiograms of 47 children with FD (20 boys, median age at first audiogram 12.0 (range 5.1–18.0) years) were analyzed. At baseline, slight/mild or moderate to severe HL was present in three children (6.4%, 2 boys). Follow-up measurements showed that three additional children developed HL before the age of 18. Of these six children, five had sensorineural HL, most likely caused by FD. Compared to healthy children (zero dB HL), FD children showed increased hearing thresholds at all frequencies (p < 0.01), which was most prominent at ultra-high frequencies (>8 kHz). Hearing sensitivity at these ultra-high frequencies deteriorated in a period of 5 years of follow-up. CONCLUSION: A minority of children with FD show slight/mild or moderate to severe HL, but their hearing thresholds are poorer than the reference values for normal-hearing children. Clinical trials in FD children should demonstrate whether HL can be prevented or reversed by early treatment and should specifically study ultra-high frequencies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10545-017-0051-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-55791382017-09-18 Hearing loss in children with Fabry disease Suntjens, E. Dreschler, W. A. Hess-Erga, J. Skrunes, R. Wijburg, F. A. Linthorst, G. E. Tøndel, C. Biegstraaten, M. J Inherit Metab Dis Original Article BACKGROUND: Hearing loss (HL) is a well-known feature of Fabry disease (FD). Its presence and characteristics have mainly been studied in adult patients, while only limited data are available on the presence and degree of HL in children with FD. This prompted us to study hearing sensitivity in pediatric FD patients. METHODS: All available audiograms of the Dutch and Norwegian children with FD were retrospectively collected. First, hearing sensitivity was determined by studying hearing thresholds at low, high, and ultra-high frequencies in children with FD and comparing them to zero dB HL, i.e., healthy children. In addition, the presence and type of slight/mild HL (defined as hearing thresholds at low frequencies of 25–40 dB HL) and moderate to severe HL (hearing thresholds >40 dB HL) at first visit were analyzed. If available, follow-up data were used to estimate the natural course of hearing sensitivity and HL in children with FD. RESULTS: One-hundred-thirteen audiograms of 47 children with FD (20 boys, median age at first audiogram 12.0 (range 5.1–18.0) years) were analyzed. At baseline, slight/mild or moderate to severe HL was present in three children (6.4%, 2 boys). Follow-up measurements showed that three additional children developed HL before the age of 18. Of these six children, five had sensorineural HL, most likely caused by FD. Compared to healthy children (zero dB HL), FD children showed increased hearing thresholds at all frequencies (p < 0.01), which was most prominent at ultra-high frequencies (>8 kHz). Hearing sensitivity at these ultra-high frequencies deteriorated in a period of 5 years of follow-up. CONCLUSION: A minority of children with FD show slight/mild or moderate to severe HL, but their hearing thresholds are poorer than the reference values for normal-hearing children. Clinical trials in FD children should demonstrate whether HL can be prevented or reversed by early treatment and should specifically study ultra-high frequencies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10545-017-0051-5) contains supplementary material, which is available to authorized users. Springer Netherlands 2017-05-31 2017 /pmc/articles/PMC5579138/ /pubmed/28567540 http://dx.doi.org/10.1007/s10545-017-0051-5 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Suntjens, E.
Dreschler, W. A.
Hess-Erga, J.
Skrunes, R.
Wijburg, F. A.
Linthorst, G. E.
Tøndel, C.
Biegstraaten, M.
Hearing loss in children with Fabry disease
title Hearing loss in children with Fabry disease
title_full Hearing loss in children with Fabry disease
title_fullStr Hearing loss in children with Fabry disease
title_full_unstemmed Hearing loss in children with Fabry disease
title_short Hearing loss in children with Fabry disease
title_sort hearing loss in children with fabry disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579138/
https://www.ncbi.nlm.nih.gov/pubmed/28567540
http://dx.doi.org/10.1007/s10545-017-0051-5
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