Recurrent neural tube defects associated with partial trisomy 2p22-pter: Report of two siblings and review of the literature

被引:0
作者
Doray, B
Favre, R
Gasser, B
Girard-Lemaire, F
Schluth, C
Flori, E
机构
[1] Hop Hautpierre, Lab Cytogenet, F-67098 Strasbourg, France
[2] SIHCUS, CMCO, Serv Gynecol Obstet, Schiltigheim, France
[3] Hop Civil, Serv Anat Pathol, Strasbourg, France
来源
GENETIC COUNSELING | 2003年 / 14卷 / 02期
关键词
anencephaly; craniorachischisis; neural tube defects; partial trisomy 2p;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recurrent neural tube defects associated with partial trisomy2p22-pter: report of two siblings and review of the literature: We report on two male siblings with partial trisomy 2p22-pter and partial monosomy 15q26-qter resulting from a maternally derived translocation t(2; 15) (p22;q26). Both fetuses had different neural tube defects (craniorachischisis in the first fetus and anencephaly in the second fetus) which were detected by sonographic examination at the end of the first trimester of pregnancy. This report demonstrates the importance of chromosomal analysis in the etiologic exploration of neural tube defects and supports the importance of 2p24 triplication in neural tube development.
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页码:165 / 172
页数:8
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