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1.
Chinese Journal of Medical Genetics ; (6): 505-507, 2004.
Article in Chinese | WPRIM | ID: wpr-328838

ABSTRACT

<p><b>OBJECTIVE</b>To establish an effective laboratory examination system for carrier detection and prenatal diagnosis of haemophilia A (HA).</p><p><b>METHODS</b>Twenty-five carriers of severe HA were directly detected by long-distance PCR (LD-PCR) in search of the factor FVIII (FVIII) gene inversion. Prenatal diagnosis was carried out using pregnant woman's venous blood sample, husband's venous blood sample and fetal navel venous sample at 20-24 weeks of gestation. The plasma coagulation factor VIII activity (FVIII:C) was detected by one-stage method. The concentration of von Willbrand factor (Vwf) was assayed by ELISA. Prenatal diagnosis was finally made by LD-PCR. The results of LD-PCR were proved by DNA sequencing.</p><p><b>RESULTS</b>Eight out of 25 cases were diagnosed as having FVIII geneinversion. Four of these 8 carriers underwent the LD-PCR for prenatal diagnosis, and 2 of them had to terminate pregnancy because their fetuses were diagnosed as having HA. The other two carriers were finally diagnosed to have normal fetuses by combined use of LD-PCR with plasma FVIII:C, vWF in pregnant woman's venous blood, husband's venous blood and fetal navel venous blood, and the one-year follow-up study demonstrated that the babies were normal and living well.</p><p><b>CONCLUSION</b>LD-PCR technique was adopted in this study to detect the factor VIII gene inversion; it could accurately and rapidly diagnose the severe cases of HA and could be used for the HA carriers in need of pregnant diagnosis.</p>


Subject(s)
Female , Humans , Pregnancy , Factor VIII , Genetics , Hemophilia A , Diagnosis , Genetics , Polymerase Chain Reaction , Methods , Prenatal Diagnosis , Methods , Reproducibility of Results
2.
Journal of Experimental Hematology ; (6): 390-392, 2003.
Article in Chinese | WPRIM | ID: wpr-355639

ABSTRACT

The aim of current study was to detect intron 22 inversion of factor VIII gene in severe hemophilia A (HA) patients and screen the carriers of the gene inversion. Fifty-five cases of severe HA were involved and factor VIII gene inversion was detected and identified by long distance-PCR (LD-PCR) and 0.6% agarose gel electrophoresis. The 11 kb and 12 kb bands indicate the factor VIII gene inversion and non-inversion, respectively. Occurring of both 11 kb and 12 kb bands indicates a carrier of the inversion. The results showed that factor VIII gene inversion existed in 22 out of 55 cases, which accounted for about 40% of total detected patients. Five carriers of factor VIII gene inversion were diagnosed from the members in 15 families. In conclusion, LD-PCR assay is a simple, rapid and accurate method for detection of factor VIII gene inversion, and this approach is helpful in screening, carrier testing, and prenatal diagnosis of severe hemophilia A.


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Humans , Infant , Male , Antigens , Chromosome Inversion , Factor VIII , Genetics , Hemophilia A , Blood , Genetics , Polymerase Chain Reaction , Methods , von Willebrand Factor , Allergy and Immunology
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