Hearing in adults with Pompe disease

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Abstract

Hearing loss has been recognized as an important cause of morbidity in infants with Pompe disease, a metabolic disorder caused by deficiency of acid á-glucosidase. It is unknown whether hearing is also affected in adult Pompe patients. We have studied the prevalence, severity, and type of hearing loss in 58 adult patients using tympanometry and pure-tone audiometry. Compared to normative data (International Organisation for Standardisation standard 7029), 72% of patients had impaired hearing thresholds at one or more frequencies in at least one ear. All measured frequencies were equally affected. All patients had a sensorineural type of hearing loss, pointing to cochlear or retrocochlear pathology. Categorised according to the standards of the World Health Organisation 21% of patients had a clinically relevant hearing loss (16% slight, 3% moderate, 2% profound). Though this suggests that hearing loss occurs in a considerable number of patients with Pompe disease, this prevalence is similar to that in the general population. Therefore, we conclude that hearing loss is not a specific feature of Pompe disease in adults. © 2011 SSIEM and Springer.

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APA

Van Der Beek, N. A. M. E., Verschuure, H., Reuser, A. J. J., Van Der Ploeg, A. T., Van Doorn, P. A., & Poublon, R. M. L. (2012). Hearing in adults with Pompe disease. Journal of Inherited Metabolic Disease, 35(2), 335–341. https://doi.org/10.1007/s10545-011-9396-3

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