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Published in: Journal of Inherited Metabolic Disease 5/2017

Open Access 01-09-2017 | Original Article

Hearing loss in children with Fabry disease

Authors: E. Suntjens, W. A. Dreschler, J. Hess-Erga, R. Skrunes, F. A. Wijburg, G. E. Linthorst, C. Tøndel, M. Biegstraaten

Published in: Journal of Inherited Metabolic Disease | Issue 5/2017

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Abstract

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.
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Metadata
Title
Hearing loss in children with Fabry disease
Authors
E. Suntjens
W. A. Dreschler
J. Hess-Erga
R. Skrunes
F. A. Wijburg
G. E. Linthorst
C. Tøndel
M. Biegstraaten
Publication date
01-09-2017
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 5/2017
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-017-0051-5

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