CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY MAPS TO CHROMOSOME-19Q12

被引:519
作者
TOURNIERLASSERVE, E
JOUTEL, A
MELKI, J
WEISSENBACH, J
LATHROP, GM
CHABRIAT, H
MAS, JL
CABANIS, EA
BAUDRIMONT, M
MACIAZEK, J
BACH, MA
BOUSSER, MG
机构
[1] HOP NECKER ENFANTS MALAD,INSERM,U12,UNITE RECH HANDICAPS GENET ENFANT,PARIS,FRANCE
[2] INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC,F-75724 PARIS,FRANCE
[3] GENETHON,F-91000 EVRY,FRANCE
[4] CEPH,INSERM,U358,F-75010 PARIS,FRANCE
[5] HOP ST ANNE,SERV NEUROL,F-75674 PARIS 14,FRANCE
[6] HOP QUINZEVINGTS,SERV NEURORADIOL,PARIS,FRANCE
[7] HOP ST ANTOINE,SERV ANAT PATHOL,F-75571 PARIS 12,FRANCE
[8] HOP ST ANTOINE,SERV NEUROL,F-75571 PARIS 12,FRANCE
关键词
D O I
10.1038/ng0393-256
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) has been recently reported as a cause of stroke. It is characterized, in the absence of hypertension, by recurrent subcortical ischaemic strokes, starting in early or midadulthood and leading in some patients to dementia. Magnetic resonance imaging and pathological examination show numerous small subcortical infarcts and a diffuse leukoencephalopathy underlaid by a non-arteriosclerotic, non-amyloid angiopathy. We performed genetic linkage analysis in two unrelated families and assigned the disease locus to chromosome 19q12. Multilocus analysis with the location scores method established the best estimate for the location of the affected gene within a 14 centimorgan interval bracketed by D19S221 and D19S222 loci.
引用
收藏
页码:256 / 259
页数:4
相关论文
共 17 条
[1]  
BAUDRIMONT M, IN PRESS STROKE
[2]   CRITERIA FOR THE DIAGNOSIS OF ISCHEMIC VASCULAR DEMENTIA PROPOSED BY THE STATE OF CALIFORNIA ALZHEIMERS-DISEASE-DIAGNOSTIC-AND-TREATMENT-CENTERS [J].
CHUI, HC ;
VICTOROFF, JI ;
MARGOLIN, D ;
JAGUST, W ;
SHANKLE, R ;
KATZMAN, R .
NEUROLOGY, 1992, 42 (03) :473-480
[3]  
Davous P, 1991, REV NEUROL-FRANCE, V5, P376
[4]  
HACHINSKI VC, 1975, ARCH NEUROL-CHICAGO, V32, P637
[5]  
LATHROP GM, 1985, AM J HUM GENET, V37, P482
[6]   A FAMILIAL DISORDER WITH SUBCORTICAL ISCHEMIC STROKES, DEMENTIA, AND LEUKOENCEPHALOPATHY [J].
MAS, JL ;
DILOUYA, A ;
DERECONDO, J .
NEUROLOGY, 1992, 42 (05) :1015-1019
[7]  
MUDD SH, 1989, METABOLIC BASIS INHE, V1, P693
[8]   MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKELIKE EPISODES - A DISTINCTIVE CLINICAL SYNDROME [J].
PAVLAKIS, SG ;
PHILLIPS, PC ;
DIMAURO, S ;
DEVIVO, DC ;
ROWLAND, LP .
ANNALS OF NEUROLOGY, 1984, 16 (04) :481-488
[9]  
PERICAKVANCE MA, 1991, AM J HUM GENET, V48, P1034
[10]   INFARCTS OF UNDETERMINED CAUSE - THE NINCD STROKE DATA-BANK [J].
SACCO, RL ;
ELLENBERG, JH ;
MOHR, JP ;
TATEMICHI, TK ;
HIER, DB ;
PRICE, TR ;
WOLF, PA .
ANNALS OF NEUROLOGY, 1989, 25 (04) :382-390