Term
Given the Etiology, List the Coagulation Disorder associated with it:
Toxic damage to endothelial cell allows platelets to come into contact with vWF causing platelet clumps |
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Definition
| Thrombocytic Thrombocytopenic Purpura (TTP) & Hemolytic Uremic Syndrome (HUS) |
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Term
Given the Etiology, List the Coagulation Disorder associated with it:
Defective Glycoprotein 1b inhibits platelets adhesion to vWF |
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Definition
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Term
Given the Etiology, List the Coagulation Disorder associated with it:
Defective Glycoprotein IIb/IIIa inhibits platelet aggregation |
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Definition
| Glanzmann's Thrombasthenia |
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Term
Given the Etiology, List the Coagulation Disorder associated with it:
Decreased Number of platelet dense granules |
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Definition
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Term
| Is Thrombocytic Thrombocytopenic Purpura (TTP) typically seen in adults or children? |
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Definition
| Adults, not usually associated with infection |
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Term
| Is Hemolytic Uremic Syndrome (HUS) typically seen in adults or children? |
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Definition
| Children after infection, especially E. Coli O157:H7 |
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Term
Given the following Test Results, List the Coagulation Disorder often associated with it:
DECREASED Platelet Count; Schistocytes; Coagulation tests usually NORMAL or Slightly ABNORMAL; Evidence of intravascular hemolysis |
|
Definition
| Thrombocytic Thrombocytopenic Purpura (TTP) & Hemolytic Uremic Syndrome (HUS) |
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Term
True or False:
Bruising, bleeding, kidney damage, and neurologic symptoms are all associated with Thrombocytic Thrombocytopenic Purpura (TTP) & Hemolytic Uremic Syndrome (HUS). |
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Definition
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Term
| How would/should you treat Thrombocytic Thrombocytopenic Purpura (TTP) & Hemolytic Uremic Syndrome (HUS)? |
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Definition
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Term
Given the Etiology, List the Coagulation Disorder associated with it:
Decreased ATP and ADP in Platelet |
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Definition
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Term
Is the following Coagulation Disorder Acquired or Genetic:
Bernard Soulier Disorder |
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Definition
|
|
Term
Is the following Coagulation Disorder Acquired or Genetic:
Glanzmann's Thrombasthenia |
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Definition
|
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Term
Is the following Coagulation Disorder Acquired or Genetic:
Wiskott-Aldrich Syndrome |
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Definition
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Term
Is the following Coagulation Disorder Acquired or Genetic:
Storage Pool Disease |
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Definition
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|
Term
| Is the Platelet count and morphology Normal, Increased, or Decreased for Glanzmann's Thrombasthenia? |
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Definition
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Term
True or False:
Bernard Soulier Disorder & Glanzmann's Thrombasthenia are Rare Conditions |
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Definition
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|
Term
Given the test results, List the Coagulation Disorder:
DECREASED Platelet Count with GIANT PLATELETS |
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Definition
|
|
Term
True or False:
Bernard Soulier Disorder has ABNORMAL PLT Aggregation with Ristocetin |
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Definition
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Term
Which Coagulation Disorder does the following Clinical description associate with:
Bleeding due to thrombocytopenia |
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Definition
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|
Term
Given the Test Results, Which Coagulation Disorder is associated with it:
INCREASED Bleeding Time; |
|
Definition
| Glanzmann's Thrombasthenia |
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|
Term
True or False:
Platelets DON'T Aggregate with ANY agonists EXCEPT for Ristocetin |
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Definition
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|
Term
Which Coagulation Disorder is the following Clinical Description associated with:
Clot Retraction Absent; Bleeding |
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Definition
| Glanzmann's Thrombasthenia |
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