Hemophilia (Inherited Bleeding Disorder)
Description
A bleeding disorder that is caused by several blood clotting factor deficiencies. Classic Hemophilia, or Hemophilia A, is caused by a deficiency of factor VIII. Hemophilia B, (Christmas disease), occurs with a deficiency of factor IX. These diseases are usually genetic and usually occur only in males. New cases can arise in families with no history of the disorder. Hemophilia can cause dangerous episodes of bleeding.
Symptoms
Blood in stool, easy bruising, heavy periods, bleeding gums, bleeding in joints.
Tests
A history and physical exam will be performed. Factor studies are completed to diagnose the specific clotting disorder.
- CBC
- Chem 12
Treatment
Therapy is determined by the type of hemophilia, the severity of the clotting deficiency, and the symptoms being experienced. The goal is to stop the bleeding, and replace the needed blood factor. For more information contact: National Hemophilia Foundation: (800)424-2634
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- Family Practice
- Hematology and Oncology
- Internal Medicine
- Pediatric Hematology and Oncology
- Pediatrics
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