@article{theodoridou2015pyruvate,
  title = {Pyruvate Kinase Deficiency along with Detection of Plasminogen Activator Inhibitor (PAI-1) 4G/4G Homozygous Genotype in Pregnancy},
  author = {Stamatia Theodoridou and Leonidas Zepiridis and Alexandra Agapidou and Theodoros Theodoridis and Timoleon - Achilleas Vyzantiadis},
  year = 2015,
  url = {https://ibimapublishing.com/articles/GYNE/2015/744272/},
  journal = {Obstetrics & Gynecology: An International Journal},
  volume = 2015 (2015),
  pages = 5,
  doi = 10.5171/2015.744272,
  abstract = {The most frequent enzyme abnormality of the glycolytic pathway which causes hereditary non-spherocytic hemolytic anemia is red cell pyruvate kinase (PK) deficiency.The disease is transmitted as an autosomal recessive trait. The case of a successful pregnancy in a 38 year- old woman with Pyruvate Kinase deficiency along with detection of plasminogen activator inhibitor (PAI-1) 4G/4G homozygous genotype is reported. The pregnancy was uneventful and a healthy girl was born.},
  keywords = {Genetic Counseling, Hematologic and Clotting Problems, Recurrent pregnancy loss},
  note = Article ID: 744272
}