First trimester prenatal diagnosis of haemophilia A using factor VIII gene probe

Jinrui Idengaku Zasshi. 1989 Jun;34(2):135-41. doi: 10.1007/BF01912482.

Abstract

Accurate first-trimester prenatal diagnosis was achieved in a Japanese haemophilia A family by the use of a restriction fragment length polymorphism (RFLP) located within the F.VIII gene. Since the pregnant woman's heterozygosity for BclI polymorphism in F.VIII/intron 18 (F8A) probe was informative, chorionic villus sampling (CVS) was performed at 9 weeks of gestation. Restriction analysis showed that the fetus was heterozygous for the BclI site and had received a normal paternal X chromosome (0.9 kb) and a normal maternal X (1.2 kb). Therefore, we concluded that the fetus was a non-carrier female. Pregnancy went to term and woman gave birth to an apparently healthy female. At one week after birth a coagulation study confirmed that the newborn infant is not a carrier. The first-trimester prenatal diagnosis of haemophilia A is possible by CVS due to a RFLP in the F.VIII gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Southern
  • Factor VII / genetics*
  • Female
  • Hemophilia A / diagnosis*
  • Humans
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length*
  • Pregnancy
  • Pregnancy Trimester, First
  • Prenatal Diagnosis*

Substances

  • Factor VII