HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A

Thromb Haemost. 2005 Apr;93(4):787-8.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Fetal Growth Retardation / etiology*
  • Fetal Growth Retardation / genetics
  • HELLP Syndrome / complications
  • HELLP Syndrome / etiology*
  • HELLP Syndrome / genetics
  • Homozygote
  • Humans
  • Polymorphism, Single Nucleotide*
  • Pre-Eclampsia / complications
  • Pregnancy
  • Prothrombin / genetics*
  • Thrombophilia / complications

Substances

  • Prothrombin