Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24

被引:152
作者
Strautnieks, SS
Kagalwalla, AF
Tanner, MS
Knisely, AS
Bull, L
Freimer, N
Kocoshis, SA
Gardiner, RM
Thompson, RJ
机构
[1] UNIV LONDON UNIV COLL,SCH MED,RAYNE INST,DEPT PEDIAT,LONDON WC1E 6JJ,ENGLAND
[2] KING FAHAD HOSP,RIYADH,SAUDI ARABIA
[3] SHEFFIELD CHILDRENS HOSP,SHEFFIELD,S YORKSHIRE,ENGLAND
[4] DENVER AURORA PATHOL ASSOCIATES,DENVER,CO
[5] UNIV CALIF SAN FRANCISCO,DEPT PSYCHIAT,SAN FRANCISCO,CA 94143
[6] CHILDRENS HOSP PITTSBURGH,PITTSBURGH,PA 15213
基金
英国惠康基金;
关键词
D O I
10.1086/515501
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Progressive familial intrahepatic cholestasis (PFIC; OMIM 211600) is the second most common familial cholestatic syndrome presenting in infancy. A locus has previously been mapped to chromosome 18q21-22 in the original Byler pedigree, This chromosomal region also harbors the locus for benign recurrent intrahepatic cholestasis (BRIC) a related phenotype. Linkage analysis in six consanguineous PFIC pedigrees from the Middle East has previously excluded linkage to chromosome 18q21-22, indicating the existence of locus heterogeneity within the PFIC phenotype, By use of homozygosity mapping and a genome scan in these pedigrees, a locus designated ''PFIC2'' has been mapped to chromosome 2q24. A maximum LOD score of 8.5 was obtained in the interval between marker loci D2S306 and D25124, with all families linked.
引用
收藏
页码:630 / 633
页数:4
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