Treating Hemophilia in Women

Hemophilia is a genetic disorder caused due to a mutation in the genes. This disorder can be inherited or can be the result of a new mutation. Hemophilia is more prevalent in men than women, since it is an X-linked recessive trait. The defected X chromosome is deficient in blood clotting protein, which disables the blood from thickening and coagulating during an injury, bruise or trauma. To further understand the reason of why hemophilia in women is a rarity, we would have to know about the XX chromosomes and the XY chromosomes. There are 24 pairs of chromosomes in humans. Out of which one... Read More

Gene Therapy for Hemophilia

Hemophilia is a genetic bleeding disorder where the blood of the patient does not clot during an injury or trauma. This is due to a deficiency or absence of blood clotting protein in the blood. There are twelve clotting factors in the human body. Two blood clotting proteins, a deficiency in either causes hemophilia are factor VIII and factor IX. A deficiency in factor VIII results in hemophilia A while that of factor IX results in Hemophilia B. Since no permanent cure for hemophilia is available patients have to undergo regular infusions which are painful, expensive and if the infusion is... Read More

Hemophilia Definition, Causes, and Treatment

The word hemophilia definition literally means “lover of blood”. That human have 23 pairs of chromosomes. Out of which one pair of chromosome is responsible for determining the sex of an individual, these are called sex chromosomes. While men have a combination of XY chromosomes, females are XX. Patients suffering from Hemophilia have a faulty X- chromosome this can be inherited from either parents or can be the caused due a new mutation. The haemophilic X chromosome does not contain blood clotting protein, in turn not coagulating the blood in case the patient bleeds. This is the... Read More

Treatment for Hemophilia

Before the treatment for hemophilia, its diagnosis is important. The kind of hemophilia and for its severity to be ascertained, the patient will have to undergo certain tests that would include measuring the clotting factors in the blood and their activity. It could also include examine the family history with respect to hemophilia. Depending upon these tests the severity of hemophilia can be decided upon. Individuals with hemophilia have been known to bleed profusely and for a prolonged period.  Soft tissues and areas with thin fibrin are more prone to such bleeds and allow easy injuries. ... Read More

Hemophilia A Treatment

Hemophilia A is a genetic disorder. It caused due to an alteration in the genes which disables the blood from clotting. Clotting disability occurs due either an absence of clotting factor or a deficiency. Depending upon the deficiency, hemophilia can be classified as mild, moderate or severe. A deficiency of clotting factor VIII causes hemophilia A. Hemophilia a treatment has come a long way. From infusion of fresh blood into the patient to the home therapy solutions, these advancements have certainly made living with hemophilia relatively better for the patients. Today, for hemophilia... Read More

Improved Hemophilia B Treatment

Hemophilia is caused due to an alteration in the genes which disables the blood from clotting. This is a genetic disease. Hemophilia B is less frequent. While hemophilia A occurs in about 1 male out of 5000, hemophilia B occurs in 1 male out of 20000. Clotting disability occurs due either an absence of clotting factor or a deficiency. Depending upon the deficiency, hemophilia can be classified as mild, moderate or severe. A deficiency of clotting factor IX causes hemophilia B. Symptoms of hemophilia b is the same as that for hemophilia a and so it the treatment. Hemophilia b treatment has... Read More