Hemophilia differential diagnosis: Difference between revisions
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==Differentiating Hemophilia with other Diseases== | ==Differentiating Hemophilia with other Diseases== | ||
*[[Von Willebrand Disease]] | |||
*[[Vitamin K deficiency]] or [[Warfarin]] | |||
*Lupus Anticoagulant | |||
*[[Heparin]] Administration | *[[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<ref>{{Cite web | title =Wikipedia Hemophilia Differential diagnosis| url =https://en.wikipedia.org/wiki/Haemophilia }}</ref> | |||
==References== | ==References== | ||
Revision as of 18:03, 1 September 2015
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Hemophilia Microchapters |
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Hemophilia differential diagnosis On the Web |
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American Roentgen Ray Society Images of Hemophilia differential diagnosis |
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Risk calculators and risk factors for Hemophilia differential diagnosis |
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 staged, 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
- Von Willebrand Disease
- 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]