Hemophilia differential diagnosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]
Overview
Hemophilia must be differentiated from other diseases that lead to spontaneous bleeding and bleeding following injuries or surgery such as Von Willebrand disease, liver failure-early or end stage, thrombocytopenia, vitamin K deficiency, disseminated intravascular coagulation, uremia, congenital afibrinogenemia, factor V deficiency, factor X deficiency as seen in amyloid purpura, glanzmann's thrombasthenia, bernard-soulier syndrome, factor XII deficiency and C1INH deficiency.
Differentiating Hemophilia with other Diseases
- Vitamin K deficiency or Warfarin
- Lupus Anticoagulant
- Heparin Administration
- Disseminated Intravascular Coagulation
- Dysfibrinogenemia
- Thrombocytopenia
- Early liver failure
- End-staged liver failure
- Uremia
- Congenital afibrinogenemia
- Factor V deficiency
- Amyloid purpura
- Glanzmann's thrombasthenia
- Bernard-soulier syndrome
- Factor XII deficiency
- C1INH deficiency[1]