Detection and genetic counseling of F8 gene inversions for patients with severe hemophilia A / 中华医学遗传学杂志

ABSTRACT

<p><b>OBJECTIVE</b>Inversions of intron 1 (Inv1) or intron 22 (Inv22) of the coagulation factor VIII gene (F8) may be found in 40%-50% of patients with severe hemophilia A. Such inversions cannot be detected by conventional sequencing. Due to homologous recombination, family-based linkage analysis may yield false positive or false negative results. In this study, Inverse-shifting PCR (IS-PCR) was used to detect potential inversions in two families affected with hemophilia A.</p><p><b>METHODS</b>Peripheral venous blood, fetal amniotic fluid and fetal chorionic cells were harvested for genome DNA extraction. IS-PCR was used to detect Inv1 or Inv22 detection or its subtypes.</p><p><b>RESULTS</b>IS-PCR has accurately detected Inv22 and Inv1 in both families and verified the subtypes of Inv22.</p><p><b>CONCLUSION</b>Carriers of Inv22 or Inv1 may be precisely detected with IS-PCR. The results have provided valuable information for genetic counseling and prenatal diagnosis for the affected families.</p>