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Causes of Abnormal Screening Results

Causes of Abnormal Screening Results | Specimen Collection and Transport Issues | Medication | Pathologic Conditions | Factor Deficiencies | Factor Inhibitors

Factor Deficiencies

Factor Deficiency

Cases per Million Individuals1

Screening Tests

Specific Factor Level Test Number

Comments

vWF

>100

vWF Profile

084715

aPTT can sometimes be extended. The aPTT should not be used to screen for von Willebrand disease (vWD) although it can sometimes be prolonged in vWD.

XII

 

aPTT

086322

It should be noted that factor XII deficiency is quite common but is not associated with bleeding.

VIII

60-100

aPTT

086264

Affects males predominantly. Congenital factor VIII deficiency (hemophilia A) affects males predominantly; factor VIII is often decreased in vWD. vWD has an autosomal mode of inheritance and, therefore, affects both sexes.

IX

10-20

aPTT

086298

Affects males predominantly.

XI

1

aPTT

 

Congenital factor XI deficiency (hemophilia C) has an autosomal mode of inheritance and, therefore, affects both sexes.

Fibrinogen

1

aPTT, PT

001610

 

II

<0.5

aPTT, PT

086231

 

V

<0.5

aPTT, PT

086249

The PT is generally more sensitive to deficiency of factor V than is the aPTT.

VII

<0.5

PT

800599

 

X

<0.5

aPTT, PT

086306

The PT is generally more sensitive to deficiency of factor X than is the aPTT.

XIII

<0.5

 

086330

Both PT and aPTT will be normal. Must test directly

More information about clinical aspects and testing for individual factor deficiencies can be found under the individual test descriptions.

References

 

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