Hemophilia
Hemophilia is a rare disorder in which a person’s blood is not able to clot properly, resulting in unusually easy and prolonged bleeding.
There are several types of hemophilia, each characterized by a deficiency, or lack, of a specific clotting factor protein. The most common form is hemophilia A, followed by hemophilia B. Both of these types primarily affect boys and men. Almost all cases of hemophilia are caused by mutations in a gene that provides instructions for making a clotting factor protein.
No cure exists for hemophilia, but a number of treatments are available that can help to minimize and control bleeding in patients. While historically most people with hemophilia have not survived to adulthood, with modern medical care, individuals born with the condition in the 21st century now have a near-normal life expectancy.
Learn more about hemophilia by heading to Hemophilia News Today, a Bionews brand.
Recent Posts
- Long-term hetrombopag safe, effective for ITP in children: Study
- von Willebrand patients see major drop in bleeds with Wilate use in trial
- Hidden HIV infection discovered following rare blood disorder relapse
- For me, the start of an ITP flare comes with clear signs
- Managing clot risk is critical in adults with immune thrombocytopenia
