GENETIC-HETEROGENEITY OF POLYCYSTIC KIDNEY-DISEASE IN BULGARIA

被引:0
|
作者
BOGDANOVA, N
DWORNICZAK, B
DRAGOVA, D
TODOROV, V
DIMITRAKOV, D
KALINOV, K
HALLMAYER, J
HORST, J
KALAYDJIEVA, L
机构
[1] UNIV MUNSTER, INST HUMAN GENET, D-48149 MUNSTER, GERMANY
[2] UNIV SOFIA, HOSP OBSTET & GYNECOL, MOLEC PATHOL LAB, BU-1431 SOFIA, BULGARIA
[3] MED UNIV PLEVEN, NEPHROL & HAEMODIALYSIS CLIN, BU-5800 PLEVEN, BULGARIA
[4] MED UNIV PLOVDIV, NEPHROL & HAEMODIALYSIS CLIN, PLOVDIV, BULGARIA
[5] MED UNIV SOFIA, DEPT MED STAT, SOFIA, BULGARIA
[6] STANFORD UNIV, DEPT GENET, PALO ALTO, CA 94304 USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Linkage analysis was performed on 22 Bulgarian families with polycystic kidney disease (PKD) ascertained through the hemodialysis centers of two medical schools, A total of 128 affected and 59 unaffected individuals, and 54 spouses have been investigated using eight polymorphic markers linked to PKD1 and nine markers to PKD2. The results demonstrate locus heterogeneity with 0.67 as the maximum likelihood value of alpha, i,e., the proportion of families linked to PKD1. In five families, the results suggest linkage to PKD2, and observed recombinants place the gene between loci D4S1544 and D4S1542. In one family, two double recombinants for closely linked markers on chromosome 16 and on chromosome 4 give evidence for the lack of linkage to either PKD1 or PKD2, thus suggesting the involvement of a third locus. Analysis of clinical data in the PKD1 group versus the unlinked group shows no significant differences in the severity of the disease.
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页码:645 / 650
页数:6
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