Audiological profile in Apert syndrome

被引：15

作者：

Rajenderkumar, D ^{[1
]}

Bamiou, DE ^{[1
]}

Sirimanna, T ^{[1
]}

机构：

[1] Great Ormond St Hosp Children, Dept Audiol Med, London WC1N 3JH, England

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 2005年 / 90卷 / 06期

关键词：

D O I：

10.1136/adc.2004.067298

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Apert syndrome is one of the craniosynostosis syndromes and is commonly associated 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 obtained; 59% were males. The incidence of congenital hearing impairment was 3 - 6%. Almost all had otitis media with effusion, which tends to persist into adulthood. More than 56% developed permanent low frequency conductive hearing loss by 10-20 years of age.

引用

页码：592 / 593

页数：2

共 9 条

[1]

[Anonymous], [No title captured]

[2]

BERGSTROM L, 1972, ARCHIV OTOLARYNGOL, V96, P117

[3]

BLANK CE, 1960, ANN HUM GENET, V24, P151

[4] BIRTH PREVALENCE STUDY OF THE APERT SYNDROME [J].

COHEN, MM ;

KREIBORG, S ;

LAMMER, EJ ;

CORDERO, JF ;

MASTROIACOVO, P ;

ERICKSON, JD ;

ROEPER, P ;

MARTINEZFRIAS, ML .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 42 (05) :655-659

[5] BIRTH PREVALENCE STUDY OF THE APERT SYNDROME [J].

CZEIZEL, AE ;

ELEK, C ;

SUSANSZKY, E .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (03) :392-392

[6]

GOULD HJ, 1982, ARCH OTOLARYNGOL, V108, P347

[7] Apert syndrome and hearing loss with ear anomalies: a case report and literature review [J].

Huang, F ;

Sweet, R ;

Tewfik, TL .

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2004, 68 (04) :495-501

[8]

MCGILL T, 1991, CLIN PLAST SURG, V18, P309

[9] CONGENITAL CONDUCTIVE HEARING-LOSS IN APERT SYNDROME [J].

PHILLIPS, SG ;

MIYAMOTO, RT .

OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1986, 95 (04) :429-433

← 1 →