A COMPARISON OF THE ALLELIC FREQUENCIES OF 10 DNA POLYMORPHISMS ASSOCIATED WITH FACTOR-VIII AND FACTOR-IX GENES IN THAI AND WESTERN-EUROPEAN POPULATIONS

被引:16
作者
GOODEVE, AC
CHUANSUMRIT, A
SASANAKUL, W
ISARANGKURA, P
PRESTON, FE
PEAKE, IR
机构
[1] ROYAL HALLAMSHIRE HOSP,DEPT MED & PHARMACOL,HAEMATOL SECT,SHEFFIELD S10 2JF,S YORKSHIRE,ENGLAND
[2] RAMATHIBODI HOSP,DEPT PAEDIAT,BANGKOK 10400,THAILAND
关键词
HEMOPHILIA; CARRIER DETECTION; GENETIC COUNSELING; DNA POLYMORPHISMS; RFLP;
D O I
10.1097/00001721-199402000-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The frequency of five factor VIII gene intragenic and linked DNA polymorphisms and five factor IX gene intragenic polymorphisms was studied in Thai females. The polymorphisms in the FVIII gene were detected by restriction enzymes BclI, XbaI, BglI. and at linked loci DX13 (DXS15) and St14 (DXS52) by BglII and TaqI, respectively, and in the FIX gene by MseI, DdeI, XmnI, TaqI and HhaI. With the exception of the BglI restriction fragment length polymorphism (RFLP), which is absent in Thais, factor VIII polymorphism frequencies were similar in Thais and Caucasians. Combined use of XbaI and TaqI/St14 resulted in a heterozygosity rate of greater than 90% in Thai females. For FIX, the recently described MseI RFLP in the 5' flanking region was the most informative polymorphism in Thais, 43% of females being heterozygous. The other four polymorphisms added little to the overall heterozygosity rate. The appropriate polymorphisms were used to track defective factor VIII and IX genes through 22 Thai pedigrees with haemophilia to enable carrier status to be assigned to female family members. The information obtained during this study will form the basis for carrier detection and prenatal diagnosis of haemophilia A and B by DNA polymorphism analysis in Thailand.
引用
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页码:29 / 35
页数:7
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