Hemophilia differential diagnosis: Difference between revisions
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{{Hemophilia}} | {{Hemophilia}} | ||
{{CMG}}; {{AE}} {{Simrat}} | {{CMG}}; {{AE}} {{Simrat}} | ||
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**Bernard-soulier syndrome | **Bernard-soulier syndrome | ||
**[[Factor XII]] deficiency | **[[Factor XII]] deficiency | ||
**C1INH deficiency<ref>{{Cite web | title = Hemophilia Differential diagnosis| url =https://en.wikipedia.org/wiki/Haemophilia }}</ref> | **C1INH deficiency<ref>{{Cite web | title =Wikipedia Hemophilia Differential diagnosis| url =https://en.wikipedia.org/wiki/Haemophilia }}</ref> | ||
==References== | ==References== |
Revision as of 21:44, 31 August 2015
kipedi
Hemophilia Microchapters |
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Hemophilia differential diagnosis On the Web |
American Roentgen Ray Society Images of Hemophilia differential diagnosis |
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 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
- 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]