MICROANATOMY

Detailed explanation-1: -What is Hemophilia? Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting factors that can help to stop bleeding.

Detailed explanation-2: -Factor V Leiden thrombophilia is an inherited disorder of blood clotting . Factor V Leiden is the name of a specific gene mutation that results in thrombophilia, which is an increased tendency to form abnormal blood clots that can block blood vessels.

Detailed explanation-3: -Hemophilia is caused by the lack of clotting factor VIII or IX in the blood. In most cases, hemophilia is passed down through families (inherited). Most of the time, it is passed to male children.

Detailed explanation-4: -Hemophilia is perhaps the most well-known inherited bleeding disorder, although it is relatively rare. It affects mostly males. Many more people are affected by von Willebrand disease, the most common inherited bleeding disorder in America caused by clotting proteins.

Detailed explanation-5: -Hemophilia A: This is the most common type of hemophilia. Hemophilia B: Hemophilia B happens when you don’t have enough clotting factor 9 (factor IX.) Hemophilia C: Hemophilia C is also known as factor 11 (factor XI) deficiency. 14-Nov-2022