Hemophilia

What Increases Your Risk

Hemophilia is an inherited genetic disease. The risk of a child inheriting hemophilia depends on the parents' genetic makeup.

Sometimes, a child is born with hemophilia because part of a normal chromosome changes (mutates) in the eggs or sperm of one or both parents. Medical researchers do not yet know why this mutation occurs in some people.


Go to previous sectionGo to previous sectionGo to top of pageGo to top of pageGo to next sectionGo to next section

Author: Robin Parks, MS
Ralph Poore
Last Updated: October 12, 2007
Medical Review: Anne C. Poinier, MD - Internal Medicine
Brian Leber, MDCM, FRCPC - Hematology

© 1995-2008 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.
This information does not replace the advice of a doctor. Healthwise disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use. How this information was developed to help you make better health decisions.

Click here to learn about Healthwise
Click here to learn about Healthwise
Topic Contents
 Topic Overview
 Health Tools Click here to view Health Tools.
 Cause
 Symptoms
 What Happens
Arrow PointerWhat Increases Your Risk
 When To Call a Doctor
 Examinations and Tests
 Treatment Overview
 Prevention
 Home Treatment
 Medications
 Surgery
 Other Treatment
 Other Places To Get Help
 Related Information
 References
 Credits