Inherited Bleeding Disorder  

Hemophilia is an inherited blood disorder that causes the child to bleed uncontrollably without clotting. Hemophilia patients lack clotting factors VIII and IX, which are needed to stop bleeding. The severity of your child’s hemophilia is determined by the concentration of blood clotting factors in their blood.

There are three types of hemophilia:

  • Hemophilia A: this is the most common type of hemophilia – about 9 out of 10 patients have type A (also referred to as “classic” hemophilia). Hemophilia A patients lack the blood clotting factor VIII
  • Hemophilia B: patients with hemophilia B lack the blood clotting factor IX
  • Hemophilia C: patients with hemophilia C lack the clotting factor XI, which is the least severe type of hemophilia. Most patients don’t have issues, although they might have a higher chance of increased bleeding after surgery

Symptoms, Diagnosis and Outlook

The most common hemophilia symptom is uncontrolled – and often substantial – bleeding. Many children have a mild form of hemophilia, meaning that no one realizes there is a problem until surgery or a bleeding injury. However, in patients with severe hemophilia, bleeding can occur for no specific reason, especially in spots like your child’s head or arm and leg joints. Bleeding in the brain is a dangerous outcome from an injury or fall with hemophilia patients – make sure your child gets medical attention immediately if they hit their head.

Additional symptoms include bleeding during dental procedures, bleeding into muscles or joints and easily bruising even from minor activity.

If your child’s physician suspects that he or she has hemophilia, they will order blood tests, including a CBC, clotting factor and bleeding time test to determine how quickly your child’s blood clots.

If your child is a carrier of the hemophilia gene, their clotting factors will be normal. Still, as a carrier your child could bruise easily, have frequent nosebleeds, heavy menstrual bleeding and bleed more after an injury or surgery.

With close medical management and treatment, most children with hemophilia can enjoy a normal lifestyle. The hematology experts at Penn State Health Children’s Hospital will work with your child and your entire family to determine a treatment program that fits your child’s needs.

Our Experts in Care

The pediatric hematology experts at Penn State Health Children’s Hospital are committed to providing our patients with comprehensive, multidisciplinary hemophilia care. 

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Why Choose Penn State Health Children’s Hospital for Care

Multidisciplinary Pediatric Hemophilia Program

The Penn State Health Children’s Hospital Hemophilia Program is an important part of Pennsylvania State University’s federal and state-funded Comprehensive Hemophilia Treatment Center. We are proud to provide multidisciplinary and comprehensive care for children with inherited bleeding disorders. Our services include:

  • Diagnosis and management of hemophilia and its complications
  • Home infusion program to have your child receive factor VIII or IX
  • Physical therapy and exercise to strengthen muscles
  • Family counseling and support

Commitment to Research

Penn State Health Children’s Hospital frequently participates in clinical trials on conditions like hemophilia. For more information on clinical trials at Penn State Health Children’s Hospital, please visit StudyFinder.

Support Groups

Support groups provide children and their families an opportunity to connect with others in similar situations. Learn more about the support groups offered at Penn State Health Children’s Hospital.

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Our Convenient Locations

Find the care your family needs, close to home, at one of our many locations throughout central Pennsylvania.

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