GENETIC-STUDY OF NONSYNDROMIC CORONAL CRANIOSYNOSTOSIS

被引:278
作者
LAJEUNIE, E
LEMERRER, M
BONAITIPELLIE, C
MARCHAC, D
RENIER, D
机构
[1] HOP NECKER ENFANTS MALAD,SERV NEUROCHIRURG,ETUD MALFORMAT CRANIOFACIALES GRP,F-75743 PARIS,FRANCE
[2] HOP NECKER ENFANTS MALAD,INSERM,U393,F-75743 PARIS,FRANCE
[3] INSERM,U155,PARIS,FRANCE
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 55卷 / 04期
关键词
CRANIOSYNOSTOSIS; CORONAL SYNOSTOSIS; GENETICS; AUTOSOMAL DOMINANT; SEGREGATION ANALYSIS;
D O I
10.1002/ajmg.1320550422
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
From a series of 1265 individuals with different craniosynostoses hospitalized between 1976 and 1993, 260 probands with nonsyndromic unilateral (181) or bilateral (79) coronal synostosis were analysed. The prevalence of craniosynostoses was estimated as 1 in 2100 children, In the group of coronal synostosis, family history was obtained on 192 probands in 180 pedigrees, The male:female ratio was 1:2. The average paternal age was 32.7 +/- 6.4 years, which is significantly higher than normal. In 26 of the 180 pedigrees, a high degree of familial aggregation was observed, giving a 14.4% figure of familial cases. The bicoronal synostoses were significantly more often familial than the unicoronal synostoses. Segregation analysis of these families leads to the conclusion that coronal synostosis is transmitted as a dominant disorder with 0.60 penetrance and 61% of sporadic cases. (C) 1995 Wiley-Liss, Inc.
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页码:500 / 504
页数:5
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