HYPOFIBRINOGENEMIA
Andy Nguyen,M.D./ UT-Medical School at Houston, Pathology/
Last Revision on: 12/9/96
- Biochemical aspects:
Please refer to the section on "Afibrinogenemia" for
further information on biochemical aspects of fibrinogen.
- Pathological Basis:
- Mode of inheritance: autosomal dominant or autosomal
recessive.
- The fibrinogen level in patients with this disorder
is usually less than 100 mg/dl. They may have a mild
tendency to bleed.
- Treatment:
- Cryoprecipitate.
- Avoidance of aspirin-containing compounds.
- Dosage: the amount of fibrinogen (in mg) required can be
calculated from:
- 40*BW*(desired fibrinogen level-actual fibrinogen level)/100
- Where BW is body weight in kg
Diagnostic Criteria:
- TT:abnormal
- Fibrinogen,clottable:abnormal(but_not_absent)
- Fibrinogen,immunogenic:abnormal(but_not_absent)