Hemophilia Essay, Research Paper. Hemophilia Hemophilia is a genetically inherited hemorrhage upset which is caused when one of the plasma proteins ( needed to coagulum ) is losing or abnormally formed in the blood. The word Hemophilia comes from the Latin word hemo, intending blood and the word affection, significance: holding a inclination.
Haemophilia, or hemophilia is a group of inherited blood disorders in which the blood does not clot properly. Known as a rare disease to individuals, Haemophilia has two main inheritable types, Haemophilia and Haemophilia B. Haemophilia is due in part to defective blood vessels, coagulation mechanisms or blood platelets.
Hemophilia essays Hemophilia is a genetic bleeding disorder. People who have hemophilia have a deficiency or an absence of a coagulation protein. A blood clotting factor is deficient or absent. Bleeding is most often into joints, such as the knee, elbow, or ankle, but bleeding can occur any.
Hemophilia a Bloody Disease Hemophilia is a bleeding disorder caused by a hereditary X-linked recessive gene disorder that causes blood to be thin due to the inability to clot normally. There are two types of Hemophilia. Type one is a deficiency in clotting factor VIII and affects nearly 80 % of the cases reported.
Hemophilia occurs when a defect in the X chromosome takes place which is one of the sex chromosomes. Hemophilia affects the entire X chromosome and is inherited in an X-linked recessive pattern. Hemophilia A’s VIII is in the F8 gene which is located on xq28.
How to write and publish a research paper in Haemophilia Christine A. Lee and Samantha Gough Introduction Hemophilia is a rare disorder and therefore publication of a research paper relating to hemophilia is sometimes difficult to achieve in mainstream journals. This monograph will therefore focus on publication in the journal Haemophilia.
Haemophilia A is a bleeding disorder where a protein made by the body to help make blood clot is either partly or completely missing. This protein is called a clotting factor: with haemophilia A there is a deficiency of clotting factor VIII (eight).
One in every five thousand women is a carrier of Hemophilia A, and one in twenty thousand is a carrier for Hemophilia B. Both types are broken up into three categories based on the amount of clotting factor present in the individual’s blood. These are known as severe, moderate, and mild. In severe hemophilia, there is usually less than one.