Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT)

被引:0
作者
Calzolari, E
Bianchi, F
Dolk, H
Stone, D
Milan, M
机构
[1] CNR, IST FISIOL CLIN, I-56100 PISA, ITALY
[2] UNIV LONDON LONDON SCH HYG & TROP MED, LONDON WC1E 7HT, ENGLAND
[3] ROYAL HOSP SICK CHILDREN, DEPT CHILD HLTH, GLASGOW G3 8SJ, LANARK, SCOTLAND
[4] MINIST PUBL HLTH & ENVIRONM, INST HYG & EPIDEMIOL, BRUSSELS, BELGIUM
[5] UNIV HOSP FERRARA, FERRARA, ITALY
[6] INSERM, PARIS, FRANCE
[7] INSERM, F-13258 MARSEILLE, FRANCE
[8] UNIV HOSP, PERUGIA, ITALY
[9] UNIV PADUA, I-35100 PADUA, ITALY
[10] UNIV GRONINGEN, DEPT MED GENET, NL-9700 AB GRONINGEN, NETHERLANDS
[11] UNIV MALTA, MSIDA, MALTA
[12] UNIV BILBAO, BILBAO, SPAIN
[13] ODENSE UNIV HOSP, DK-5000 ODENSE, DENMARK
[14] INST MORPHOL PATHOL, LOVERVAL, FRANCE
[15] MINIST PUBL HLTH, LUXEMBOURG, LUXEMBOURG
[16] ROYAL LIVERPOOL UNIV HOSP, LIVERPOOL, MERSEYSIDE, ENGLAND
[17] EASTERN HLTH BOARD, DUBLIN, IRELAND
[18] UNIV COLL HOSP, GALWAY, IRELAND
[19] QUEENS UNIV BELFAST, BELFAST BT7 1NN, ANTRIM, NORTH IRELAND
[20] PROVINCIAL INST HYG, ANTWERP, BELGIUM
[21] UNIV LAUSANNE, CH-1015 LAUSANNE, SWITZERLAND
[22] UNIV HOSP, STRASBOURG, FRANCE
[23] UNIV ZAGREB, ZAGREB 41000, CROATIA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 72卷 / 01期
关键词
omphalocele; NTD; congenital anomalies; etiology;
D O I
10.1002/(SICI)1096-8628(19971003)72:1<79::AID-AJMG17>3.3.CO;2-V
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have analyzed the association between omphalocele and neural tube defects (O/NTD) previously reported in epidemiological studies of EUROCAT registry data [DoIk et al., 1991; Calzolari et al., 1995]. By examining differences in prevalence between the United Kingdom and Ireland (UKI) and Continental Europe and Malta (CEM) and differences in sex ratio, the possible etiopathogenetic differences between O/NTD association and omphalocele without NTD and NTD without omphalocele were investigated. The distribution of O/NTD cases according to NTD site in the two geographic areas shows in the UKI a tendency for omphalocele to associate with anencephaly/spina bifida and with anencephaly. In CEM centers, these types of NTD are much rarer. The pattern of other anomalies occurring in combination with O/NTD association in the same babies was also analysed. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:79 / 84
页数:6
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