Bleeding diathesis: Difference between revisions

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| rowspan="12" |Coagulation disorders
| rowspan="12" |Coagulation disorders
|Fibrinogen
|Fibrinogen deficiency
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|Prothrombin
|Prothrombin deficiency
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| rowspan="1" |Factor V
| rowspan="1" |Factor V deficiency
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| rowspan="1" |Factor VII
| rowspan="1" |Factor VII deficiency
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| rowspan="1" |Factor VIII
| rowspan="1" |Factor VIII deficiency
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| rowspan="1" |Factor IX
| rowspan="1" |Factor IX deficiency
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| rowspan="1" |Factor X
| rowspan="1" |Factor X deficiency
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| rowspan="1" |Factor XI
| rowspan="1" |Factor XI deficiency
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| rowspan="1" |Factor XII
| rowspan="1" |Factor XII deficiency
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|HK
|HK deficiency
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| rowspan="1" |Prekallikrein
| rowspan="1" |Prekallikrein deficiency
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| rowspan="1" |Factor XIII
| rowspan="1" |Factor XIII deficiency
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| rowspan="3" |[[Hemophilia]]
| rowspan="3" |[[Hemophilia]]
|Type A
|Type A deficiency
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|Type B
|Type B deficiency
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|Type C
|Type C deficiency
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Revision as of 17:43, 6 August 2018


Bleeding diathesis main page

Overview

Classification

Differential Diagnosis

Platelet disorders
Immune Thrombocytopenic Purpura
Thrombotic Thrombocytopenic Purpura
Hemolytic Uremic Syndrome
Thrombocytosis
Von Willebrand Disease
Coagulation disorders
Fibrinogen deficiency
Prothrombin deficiency
Factor V deficiency
Factor VII deficiency
Factor VIII deficiency
Factor IX deficiency
Factor X deficiency
Factor XI deficiency
Factor XII deficiency
High-molecular-weight kininogen deficiency
Prekallikrein deficiency
Factor XIII deficiency
Hemophilia
Rare diseases
Disseminated Intravascular Coagulation
Vitamin K Deficiency

Different types of Von-Willebrand diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Mehrian Jafarizade, M.D [2]

Overview

Classification

Differential Diagnosis

Platelet disorders Thrombocytopenia Infection-Induced Thrombocytopenia
Drug-Induced Thrombocytopenia
Heparin-Induced Thrombocytopenia
Immune Thrombocytopenic Purpura (ITP)
Inherited Thrombocytopenia
Thrombotic Thrombocytopenic Purpura (TTP)
Hemolytic Uremic Syndrome
Thromobcytosis Thrombocytosis in response to acute or chronic inflammation has not been associated with an increased thrombotic risk. In fact, patients with markedly elevated platelet counts (>1.5 million), usually seen in the setting of a myeloproliferative disorder, have an increased risk of bleeding. This appears to be due, at least in part, to acquired von Willebrand disease (VWD) due to platelet-VWF adhesion and removal.
Qualitative Disorders of Platelet Function Inherited Disorders of Platelet Function
Acquired Disorders of Platelet Function
von Willebrand Disease Type 1
Type 2 A
Type 2 B
Type 2 M
Type 3
Vessel wall disorders Metabolic and Inflammatory Disorders
Inherited Disorders of the Vessel Wall
Coagulation disorders Fibrinogen deficiency
Prothrombin deficiency
Factor V deficiency
Factor VII deficiency
Factor VIII deficiency
Factor IX deficiency
Factor X deficiency
Factor XI deficiency
Factor XII deficiency
HK deficiency
Prekallikrein deficiency
Factor XIII deficiency
Hemophilia Type A deficiency
Type B deficiency
Type C deficiency
Rare diseases Disseminated Intravascular Coagulation
Vitamin K Deficiency
Coagulation Disorders Associated with Liver Failure
Acquired Inhibitors of Coagulation Factors