Bleeding Disorders

Bleeding disorders are broadly classified as congenital (inherited) or acquired:

  • Congenital bleeding disorders are caused by defects or damage in a developing fetus. Congenital defects can be due to inherited abnormalities in genes or chromosomes or to intrauterine conditions, such as infections.
  • Acquired bleeding disorders are those that develop or spontaneously occur in the individual.

Von Willebrand Disease

Hemophilia A

Hemophilia B

Fibrinogen Deficiency

References
1. Ma A. Evaluation of the bleeding patient. In: Key N, Makris M, O’Shaughnessy D, Lillicrap D, editors. Practical Hemostasis and Thrombosis. 2nd ed: Wiley-Blackwell, 2009:48–60.
2. Asselta R, Duga S, Tenchini ML. The molecular basis of quantitative fibrinogen disorders. J Thromb Haemost 2006;4(10):2115-29.
3. Peyvandi F, Palla R. Fibrinogen concentrates. Clin Adv Hematol Oncol 2009;7(12):788-90.

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