Hemophilia is a group of bleeding disorders. It is caused by low amounts of specific clotting factors. These factors help to stop bleeding.

The most common types of hemophilia are:

  • Hemophilia A (classic hemophilia)—accounts for 80% of all hemophilia; caused by too little factor VIII
  • Hemophilia B (Christmas disease)—occurs in 1 in 20,000 males, caused by too little factor IX


Hemophilia is caused by a faulty gene located on the X chromosome.

Females carry 2 copies of the X chromosome. If the faulty gene is only on one X, the normal gene on the second X will take over. As a result, they will not get the disease. Instead, they are carriers of the gene. The risk for their male offspring to inherit the gene is 1 in 2 or 50%. The chance that their female offspring will inherit the gene is also 50%. These female offspring will be carriers like their mothers.

It is possible for a female to have hemophilia. For this to happen she must inherit the faulty gene from both her mother and her father.

Males carry only one X chromosome. If they get the faulty gene, the disease will develop.

It is possible for a new genetic mutation to occur. This means a person can get hemophilia even if neither parent carries a genetic mutation.

Genetic Outcome Possibilities
Fetus Chromosomes
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Risk Factors

Hemophilia mostly occurs in men. Your chances of hemophilia are also increased if you have a family member with hemophilia.



Symptoms may vary depending on the severity of the disease. Bleeding is the main symptom, which is often brought on by injury or surgery. Hemophilia may go unnoticed until the infant becomes mobile. In severe cases, bruising occurs easily, and spontaneous bleeding into joints can cause joint pain. Symptoms in mild versions of hemophilia may not appear until later in life.

Symptoms that can occur with hemophilia include:

  • Easy bruising
  • Severe nosebleeds
  • Blood in urine
  • Blood in stools
  • Heavy bleeding after minor cuts, bumps, dental work, or other trauma
  • Joint pain
  • Heavy menstrual bleeding in women who are carriers


You will be asked about your symptoms and medical history. A physical exam will be done.

Tests may include:

  • Tests to see how well your blood clots and blood tests to look for other causes of bleeding problems
  • Blood tests to measure the amounts of clotting factors present



Talk with your doctor about the best treatment plan for you. Options include:

Blood Factor Concentrate

You'll be tested often to monitor your factor levels. When your factor levels drop too low, you may be given a dose. You may also be given a dose if you are bleeding or at high risk for bleeding, such as during surgery.

Blood factor concentrate may be given through an IV. The type of blood factor that you are given depends on the type of hemophilia you have.

People with hemophilia and their families can be taught to give blood factor concentrate at home at the first signs of bleeding. This can help prevent a crisis. People with severe forms of the disease may need regular infusions.

Some patients develop an inhibitor to a particular factor. This may require treatment with other clotting factors.


Mild hemophilia A may be treated with an infusion of medication. This infusion causes the release of blood factor stored within the body on the lining of blood vessels.


The hepatitis B and hepatitis A vaccines are important. There is an increased risk of exposure to hepatitis with frequent infusions of blood products.

Bleeding Prevention

The following steps may help prevent bleeding:

  • Good dental care is important. It may decrease the risk of major dental work.
  • Be aware of the effect of high impact activities:
    • Take extra care to protect the head from injuries.
    • People with severe hemophilia should avoid activities that include a high risk of collision.
  • Avoid drugs that can also aggravate bleeding problems such as:
    • Blood thinners, such as aspirin or heparin
    • Antiplatelets, such as warfarin
    • Certain analgesics, such as nonsteroidal anti-inflammatory drugs


There are no current guidelines to prevent hemophilia. However, if you have a family history of hemophilia, genetic counselors can help you figure out what risk your potential offspring may have.

This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.

Edits to original content made by Denver Health.

a (Hemophilia A—Factor VIII Deficiency; Classic Hemophilia; Hemophilia B—Factor IX Deficiency; Christmas Disease)


American Society of Hematology http://www.hematology.org 

National Hemophilia Foundation http://www.hemophilia.org 


Caring for Kids—Canadian Paediatric Society http://www.caringforkids.cps.ca 

Network of Rare Blood Disorder Organizations http://www.hemophilia.ca 


What is hemophilia? National Heart, Lung, and Blood Institute website. Available at: http://www.nhlbi.nih.gov/health/health-topics/topics/hemophilia. Updated July 13, 2013. Accessed June 9, 2016.

Hemophilia A. EBSCO DynaMed Plus website. Available at:  http://www.dynamed.com/topics/dmp~AN~T115190/Hemophilia-A . Updated August 5, 2016. Accessed September 28, 2016.

Hemophilia B. EBSCO DynaMed Plus website. Available at:  http://www.dynamed.com/topics/dmp~AN~T113770/Hemophilia-B . Updated September 2, 2016. Accessed September 28, 2016.

10/24/2012 DynaMed's Systematic Literature Surveillance. http://www.ebscohost.com/dynamed: Broderick CR, Herbert RD, et al. Association between physical activity and risk of bleeding in children with hemophilia. JAMA. 2012 Oct 10;308(14):1452-9.

4/24/2014 DynaMed Plus Systematic Literature Surveillance.  http://www.dynamed.com/topics/dmp~AN~T113770/Hemophilia-B : US Food and Drug Administration. FDA approves first long-acting recombinant coagulation Factor IX concentrate for patients with Hemophilia B. US Food and Drug Administration website. Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm391037.htm. Published March 28, 2014. Accessed June 9, 2016.