Hemophilia A
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Hemophilia A, also called factor VIII (FVIII) deficiency or classic hemophilia, is a genetic disorder caused by missing or defective factor VIII, a clotting protein. Although it is passed down from parents to children, about 1/3 of cases are caused by a spontaneous mutation, a change in a gene. According to the US Centers for Disease Control and Prevention, hemophilia occurs in approximately 1 in 5,000 live births. There are about 20,000 people with hemophilia in the US. All races and ethnic groups are affected. Hemophilia A is four times as common as hemophilia B while more than half of patients with hemophilia A have the severe form of hemophilia.
This video in 30 seconds
This video explains hemophilia A, also called factor VIII deficiency or classic hemophilia. It describes it as a genetic disorder caused by missing or defective factor VIII, a clotting protein, notes that about a third of cases arise from a spontaneous mutation, and gives figures on how often hemophilia occurs.
Key points
- Hemophilia A is also called factor VIII deficiency or classic hemophilia
- It is caused by missing or defective factor VIII, a clotting protein
- About one third of cases are caused by a spontaneous mutation
- Hemophilia occurs in approximately 1 in 5,000 live births
- Hemophilia A is four times as common as hemophilia B
Video Overview
This video presents “Hemophilia A” — Hemophilia A, also called factor VIII (FVIII) deficiency or classic hemophilia, is a genetic disorder caused by missing or defective factor VIII, a clotting protein. Although it is passed down from parents to children, about 1/3 of cases. Whether you are preparing for a procedure, studying the technique, or learning how a condition is assessed, the recording shows the process as it is performed in practice.
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