MAPPING OF THE GENE FOR AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE (ARPKD) TO CHROMOSOME 6P21-CEN

被引:205
作者
ZERRES, K
MUCHER, G
BACHNER, L
DESCHENNES, G
EGGERMANN, T
KAARIAINEN, H
KNAPP, M
LENNERT, T
MISSELWITZ, J
VONMUHLENDAHL, KE
NEUMANN, HPH
PIRSON, Y
RUDNIKSCHONEBORN, S
STEINBICKER, V
WIRTH, B
SCHARER, K
机构
[1] HOP GATIEN CLOCHEVILLE,TOURS,FRANCE
[2] HOP GATIEN,INSERM,U129,BIOCHIM GENET LAB,F-75674 PARIS 14,FRANCE
[3] UNIV HELSINKI,DEPT MED GENET,SF-00290 HELSINKI,FINLAND
[4] UNIV BONN,INST MED STAT DOKUMENTAT & DATENVERARBEITUNG,D-53127 BONN,GERMANY
[5] FREE UNIV BERLIN,KINDERKLIN,D-14059 BERLIN,GERMANY
[6] UNIV JENA,KINDERKLIN,D-07745 JENA,GERMANY
[7] KINDERHOSP OSNABRUCK,D-49082 OSNABRUCK,GERMANY
[8] UNIV FREIBURG,MED KLIN,D-79106 FREIBURG,GERMANY
[9] UNIV CATHOLIQUE LOUVAIN,CLIN UNIV ST LUC,DEPT MED INTERNE,B-1200 BRUSSELS,BELGIUM
[10] UNIV MAGDEBURG,INST HUMANGENET,D-39120 MAGDEBURG,GERMANY
[11] UNIV HEIDELBERG,KINDERKLIN,D-69120 HEIDELBERG,GERMANY
关键词
D O I
10.1038/ng0794-429
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autosomal recessive polycystic kidney disease (ARPKD) is one of the major hereditary nephropathies in children predominantly presently in early childhood. The clinical picture is variable but there is a fatal outcome in many cases. We have performed linkage analysis in 16 ARPKD families and localized the ARPKD gene to chromosomal region 6p21-cen with no evidence for genetic heterogeneity among different clinical phenotypes. Linkage was confirmed using six adjacent microsatellite markers and the highest rod score of 7.42 was obtained with D6S272 at theta=0.00. Our findings should lead to more accurate forms of prenatal diagnosis than those currently available using ultrasound.
引用
收藏
页码:429 / 432
页数:4
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