【摘 要】
：
Apert syndrome is one of the craniosynostosis syndromes and is commonly associ ated with conductive hearing loss, but there are contradicting reports regarding
【机 构】
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Department of Audiological Medicine Royal National Throat Nose and Ear Hospital Grays Inn Road Lond
【出 处】
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世界核心医学期刊文摘(儿科学分册)
论文部分内容阅读
Apert syndrome is one of the craniosynostosis syndromes and is commonly associ ated with conductive hearing loss, but there are contradicting reports regarding the cause. Retrospective analysis of case notes of Apert syndrome patients seen between 1970 and 2003 was therefore undertaken. Seventy case notes were obtaine d; 59%were males. The incidence of congenital hearing impairment was 3.0%. Alm ost all had otitismedia with effusion, which tends to persist into adulthood. Mo re than 56%developed permanent low frequency conductive hearing loss by 10-20 years of age.
Apert syndrome is one of the craniosynostosis syndromes and is often associated with a conductive hearing loss loss, but there are contradicting reports regarding the cause. Retrospective analysis of case notes of Apert syndrome patients seen between 1970 and 2003 was therefore undertaken. Seventy case notes were obtaine d, 59% were males. The incidence of congenital hearing impairment was 3.0%. Alm ost all had otitismedia with effusion, which tends to persist into adulthood. Mo re than 56% developed permanent low frequency conductive hearing loss by 10-20 years of age.
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