General Discussion Summary Hemophilia B is a rare genetic bleeding disorder in which affected individuals have insufficient levels of a blood protein called factor IX.
Hemophilia A Hemophilia A The constant similarity between each of my sources is the fact that they each defined hemophilia; two of them explained the difference between type A and B.
It was also noted in each source that this disease is an inherited X-linked recessive trait, which makes the defective gene located on the X chromosome. Females have two X chromosomes, whereas males have only one.
However, men are not as fortunate, and if their X chromosome is affected, they will be stricken with hemophilia A. It has been triply noted that it is extremely rare for a woman to have hemophilia for the above reason, although she may be a carrier for her unborn male children.
Each source acknowledged that there is no cure, but there is treatment, which is usually self-administered several times a week. Each site did give facts and statistics, which taught me something I did not know beforehand, and even suggested, that exercise, to a degree, was good for the infected person.
I always thought that hemophiliacs needed to walk around as though inside a bubble, for fear of bumping into something and maybe even cutting themselves.
I always believed that a person suffering with this disorder would bleed vast amounts of blood if troubled by an open wound, but they only tend to bleed longer than an unaffected person. The audience these articles would attract could be parents of a child, or a relative or friend of someone that they suspect may be affected by this disorder, especially considering that mild cases may go unnoticeMM is a five years old boy who was diagnosed with Haemophilia A since six months of age.
Haemophilia Case Study: Haemophilia is the hereditary disease which is connected with the disorder of the process of coagulation; moreover, the disease is characterized with haemorrhage into joints, muscles and organs without any reason or under the impact of injury or surgical intervention. Published: Mon, 5 Dec MM is a five years old boy who was diagnosed with Haemophilia A since six months of age. He presented to the daycare of the Paediatric department with left elbow swelling for one day after hitting it against the wall while playing. Hemophilia, one of the oldest known genetic disorders, can be classified into type A, B, or C. Hemophilia A (factor VIII deficiency) is the most common form, accounting for 85% of all patients with hemophilia.
He presented to the daycare of the Paediatric department with left elbow swelling for one day after hitting it against the wall while playing. Case Studies. Case 1.
Master Spring Flower aged In this process he lost one year of academic study. At the school, boys tease him for being weak and avoiding sports and games. “The less said about it, the better”.
|More Essay Examples on Obesity Rubric Therefore, the individual male diagnosed with hemophilia suffers from some or all of the following symptoms: Childhood Obesity Obesity, in general, is a growing health concern in developed countries.|
|Case Study on Haemophilia | benjaminpohle.com||What are the different components of factor VIII?|
she replies adding “they say that the boy has hemophilia because my heart is bad. Our participation in social.
A Year-Old Man with Previously Diagnosed Hemophilia Francesca Khani1,2* and Mikhail Roshal2 CASE A year-old Middle Eastern man diagnosed with hemophilia at . FEIBA is effective and well tolerated in minor surgery Case study: 9-year-old boy with severe haemophilia A and a high-responding inhibitor 1.
(A case of severe hemophilia, psychological stress on collapse of marriage) He was diagnosed properly only when he was eleven years old. He had gone for a swim . The Case study of a boy with haemophilia is one of the most popular assignments among students' documents. If you are stuck with writing or missing ideas, scroll . Haemophilia Case Study: Haemophilia is the hereditary disease which is connected with the disorder of the process of coagulation; moreover, the disease is characterized with haemorrhage into joints, muscles and organs without any reason or under the impact of injury or surgical intervention.
Patient history. (A case of severe hemophilia, psychological stress on collapse of marriage) He was diagnosed properly only when he was eleven years old.
He had gone for a swim . Hemophilia B is caused by mutations in the F9 gene. The F9 gene is located on the X chromosome and thus is inherited as an X-linked recessive trait.
In about 30% of new cases of hemophilia B, the altered gene occurs spontaneously without a previous family history.