What is Thrombophilia and how is it diagnosed and treated?
Thrombophilia is a hereditary or acquired predisposition to develop blood clots. It is also referred to as hypercoagulation state or hypercoagulability. Below is a list of NATT resources and articles on thrombophilia and its diagnosis and treatment:
Antiphospholipid Syndrome (APS) Written by: Jan M. Pankey, M.D.
Antithrombin Deficiency An In-Depth Guide for Patients and Health Care Providers By Dr. Stephan Moll
The Evolving Story of Pregnancy Outcome, Thromboembolism and Thrombophilia
Below is a list of external resources recognized by NATT's medical scientific and advisory board:
Click on the Resource Below | PDF/Printable | Key Points |
What is thrombophilia? Who has it? How are people with thrombophilia cared for? Acquired and hereditary factors. | ||
University of Michigan Health Systems Hemophilia and Coagulation Disorders Program | Printable | What is thrombophilia? Acquired risk factors; clots and clot formation; inherited risk factors * Also in Spanish |
No | Causes, symptoms, complications, diagnosis and treatment | |
Congenital Thrombophilias; Produced by Lifeblood:; The Thrombosis Charity. | Summarizes all major congenital/inherited thrombophilias including factor V Leiden, prothrombin G20210A, protein C deficiency, protein S deficiency, antithrombin deficiency and rarer disorders like dysfibrinogenemia. Provides a general description, discussed inheritance, and implications for blood clots and pregnancy complications. |