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Algorithm Information

Identification of a Patient with a Hereditary Deficiency of Prekallikrein and/or High Molecular Weight Kininogen

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Purpose:
To evaluate a patient with a prolonged aPTT for evidence of a hereditary deficiency of prekallikrein and/or high molecular weight kininogen.
Specialty
  • Hematology Oncology
    Clinical Laboratory
Objective
  • Laboratory tests
  • Criteria for diagnosis
ICD-10
  • D68.8
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Identification of a Patient with a Hereditary Deficiency of Prekallikrein and/or High Molecular Weight Kininogen
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