Periventricular heterotopia: An X-linked dominant epilepsy locus causing aberrant cerebral cortical development

被引:248
作者
Eksioglu, YZ
Scheffer, IE
Cardenas, P
Knoll, J
DiMario, F
Ramsby, G
Berg, M
Kamuro, K
Berkovic, SF
Duyk, GM
Parisi, J
Huttenlocher, PR
Walsh, CA
机构
[1] AUSTIN HOSP,DEPT NEUROL,MELBOURNE,VIC 3084,AUSTRALIA
[2] BETH ISRAEL HOSP,CHILDRENS HOSP,DEPT PATHOL,DIV GENET,BOSTON,MA 02215
[3] UNIV CONNECTICUT,DEPT PEDIAT,FARMINGTON,CT
[4] UNIV CONNECTICUT,DEPT RADIOL,FARMINGTON,CT
[5] UNIV ROCHESTER,DEPT NEUROL,ROCHESTER,NY
[6] KOKUBU SEIKYO HOSP,DEPT NEUROL,KAGOSHIMA,JAPAN
[7] MILLENNIUM PHARMACEUT,CAMBRIDGE,MA
[8] MAYO CLIN,DEPT PATHOL ANAT,ROCHESTER,MN
[9] UNIV CHICAGO,DEPT PEDIAT,DEPT NEUROL,CHICAGO,IL 60637
关键词
D O I
10.1016/S0896-6273(00)80025-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Periventricular heterotopia (PH) involves dramatic malformations of the human cerebral cortex. Here we show that PH is closely linked to markers in distal Xq28 (maximal two-point lod score = 4.77 for F8C at theta = 0; maximal multipoint lod score = 5.37), so that affected females are obligatory mosaics for the mutation; that PH is lethal to at least some affected males; that PH malformations consist of well-differentiated cortical neurons filling the adult subependymal zone; and that individuals with PH are at high risk for epilepsy, though they have no other neurological or external stigmata. The PH gene may represent an important epilepsy susceptibility locus in addition to playing a key role in normal cortical development.
引用
收藏
页码:77 / 87
页数:11
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