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Question 1:

Can you name 3 or more complications of hemophilia?

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Question 1:

Can you name 3 or more complications of hemophilia?

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Joint swelling that can lead to damage or swelling in the muscle
Bleeding in the head and sometimes in the brain leading to brain damage
Damage to other organs in the body\n
Pain as a result of bleeding in various organs
Death can occur if the bleeding cannot be stopped or if it occurs in a vital organ such as the brain

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Question 2:

Can a person be born with hemophilia if his parents don\u2019t have the disorder?

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Question 2:

Can a person be born with hemophilia if his parents don\u2019t have the disorder?

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Answer: Yes

About one-third of babies who are diagnosed with hemophilia have no other family members with the disorder.\n

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Question 3:

Name 5 things people with

hemophilia can do to stay healthy.

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Answer:

Get an annual comprehensive checkup at a hemophilia treatment center.
Get vaccinated\u2014Hepatitis A and B are preventable.
Treat bleeds early and adequately.
Exercise and maintain a healthy weight to protect your joints.
Get tested regularly for blood-borne infections.

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Question 3:

Name 5 things people with
hemophilia can do to stay healthy.

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Question 4:

How can joint damage in a person with hemophilia be lessened?

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Answer: Preventative treatment (prophylaxis)

\n\nA CDC-sponsored randomized clinical trial found that children who were treated on a regular basis to prevent bleeding had less evidence of joint damage by 6 years of age than did those who were treated only after a bleed had started.\n

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Question 4:

How can joint damage in a person with hemophilia be lessened?

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Question 5:

Can females have symptoms of hemophilia?

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Question 5:

Can females have symptoms of hemophilia?

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Answer: Yes

\nFemales can be hemophilia carriers. A female who inherits one affected X chromosome becomes a \u201ccarrier\u201d of hemophilia. A female who is a carrier can sometimes have symptoms of hemophilia. In addition, she can pass the affected gene on to her children.\n

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Extra Credit:

What is an inhibitor?

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Answer:

About 10 \u2013 15 percent of people with hemophilia develop an antibody (called an inhibitor) that inhibits the action of the clotting factors used to treat bleeding. Treatment of bleeding becomes extremely difficult, and the cost of their care can skyrocket because more clotting factor or a different type of clotting factor is needed. Patients with inhibitors often experience increased joint disease and other complications from bleeding that result in a reduced quality of life.

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Extra Credit:

What is an inhibitor?

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To find out more, visit:

www.cdc.gov/hemophilia

National Center on Birth Defects and Developmental Disabilities

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To find out more, visit:

www.cdc.gov/hemophilia

National Center on Birth Defects and Developmental Disabilities

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To find out more, visit:

www.cdc.gov/hemophilia

National Center on Birth Defects and Developmental Disabilities

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