Hemophilia B, also known as Christmas disease, is a genetic disorder stemming from a deficiency in clotting factor IX, crucial for proper blood coagulation. Predominantly affecting males due to its X-linked recessive inheritance
Understanding the Causes of Hemophilia B
Hemophilia B is a genetic bleeding disorder caused by a deficiency in clotting factor IX. It is typically inherited through the X chromosome, primarily affecting males. Understanding its causes helps guide accurate diagnosis, early treatment, and genetic counseling.
Treatment Options for Hemophilia B
Advanced treatments like recombinant factor IX products, regarded highly for safety, are integral to routine prophylaxis, especially in children with severe forms. Further, alternative therapies like aminocaproic acid help prevent premature clot breakdown, being particularly important