Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia

J Thromb Haemost. 2012 Dec;10(12):2625-7. doi: 10.1111/jth.12031.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Antithrombins / metabolism*
  • Congenital Disorders of Glycosylation / complications
  • Congenital Disorders of Glycosylation / diagnosis*
  • Humans
  • Male
  • Thrombophilia / complications*

Substances

  • Antithrombins