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Management of hearing loss in Apert syndrome

Published online by Cambridge University Press:  08 March 2006

D Rajenderkumar
Affiliation:
Department of Audiological Medicine, Great Ormond Street Children’s Hospital, London, UK.
D Bamiou
Affiliation:
Department of Audiological Medicine, Great Ormond Street Children’s Hospital, London, UK.
T Sirimanna
Affiliation:
Department of Audiological Medicine, Great Ormond Street Children’s Hospital, London, UK.

Abstract

Background: Apert syndrome is one of the craniosynostosis syndromes, with abirth prevalence estimated to be between 9.9 and 15.5/million, and accounts for 4.5 per cent ofcraniosynostoses. Although conductive hearing loss is common in Apert syndrome there are contradicting reports regarding the cause of this hearing loss. There is also no detailed informationavailable on the management of hearing loss in Apert syndrome.

Materials and methods: A retrospective analysis of case notes of Apert syndrome patients seen between 1970 and 2003 at Great Ormond Street Children’s Hospital, London, was undertaken.

Results: Seventy case notes were obtained. The incidence of congenital hearing impairment was between 3 and 6 per cent. Almost all patients had otitis media with effusion (glue ear), which tended to persist into adult life. More than 56 per cent of cases developed permanent conductive hearing loss by 10–20 years. Repeated grommet insertion was common; even though 35 per cent had trouble with ear discharge and persistent conductive hearing loss. Statistically, grommets made no difference to the risk of developing permanent hearing loss.

Conclusion:This study, of the largest number of Apert syndrome cases assembled to date, showed that early optimization of hearing with possible hearing aids needs to be considered. Repeated grommet insertion does not help in optimizing hearing, especially if ear discharge complicates the picture.

Type
Research Article
Copyright
© 2005 Royal Society of Medicine Press

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