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Essay on therapies in hemophilia
Essay on therapies in hemophilia
Essay on therapies in hemophilia
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Today i'm going to be talking about Hemophilia and the general overview of it. I will also talk about any potential cures. I will be talking about what Hempohilia can do to your body. I will also be talking about if theres a cure or just a treatment to make it less worse. I will also be talking about how people with Hemophilia deal with this disease. I will also explain how people will benefit from extended research on thi s topic. I’ll also talk about my personal opininon on this topic and what I think about it. So for my first question I’m explaining what the characteristics of Hemophilia are. The characteristics of Hemophilia are not very deadly but can be very annoying I’ll also explan the genetic causes of this disease. The symptoms …show more content…
One way that people adapt to this activity is avoiding activitys that they know will easly bruise or cut them. For kids parents ofter will try to avoid getting household items with sharp edges. Also parents will often enroll there kid in a support group that supports there disease. So as you can see there are many ways to deal with Hemophilia. Although this disease isnt to common there still has been some new research about this topic. About 400,000 people live with hemophilia each year while there are only about 20,000 people that live with it in America. About 400 babys are born with this disease each year in the U.S. Usually only males get this disease but it is possible for women to get it. Hemophilia is also caused by a genetic mutation. So as you can see Hemophilia is not to common. Today i'm going to be talking about Hemophilia and the general overview of it. I will also talk about any potential cures. This disease has many symptoms and characteristics. This disease does not have a cure yet but there are many ways to deal with it. There are many ways to deal with Hemophialia. Henophilia is not very common and can be caused by a genetic mutation. So as you can see if you have hemophilia it can affect your life in numerous ways. However there are multiple ways to deal with it that is either stuff you can do on your own or scientific
Specific Purpose Statement: To persuade my audience to donate blood through the American Red Cross.
• Hemolytic disease of the newborn. Hemolytic disease happens when a mother 's disease fighting system (immune system) attacks her baby 's red blood cells. Proteins (antibodies) in the mother’s blood destroy the baby 's red blood cells. Two conditions can cause hemolytic disease:
Genetic disorders can be caused by many of the 46 chromosomes in human cells. This specific disorder is linked to a mutation in the long arm of the X, or 23rd chromosome. The mutation is recessive, meaning a normal X chromosome can hide it. Females have two X chromosomes allowing them to hide the mutated recessive one, making them a carrier of the gene, while males only have one X chromosome, meaning that they are unable to hide the mutation and they become effected by the disease. Therefore if a male carries the gene, he is affected because he has no way of dominating the recessive gene, but if a female carries it, she is only a carrier and has a 50/50 chance of passing it on to her baby. This may seem like a high probability however, only one in every fifty thousand male births will have this immunodeficiency disease.
Of the children of a hemophiliac male and a normal female, all the girls will be carriers and all the boys will be normal. Males cannot transmit the disability, and female carriers are free of the disease. Conventional wisdom suggests that 1 in 10,000 males in the United States have hemophilia. However, increased research and focus, on bleeding disorders in general and on bleeding disorders in women specifically, suggest a shift in what...
In the early 1980s, most people with Hemophilia were injected with “HIV”, because the factors used for treatment were isolated from injected human plasma. Since then, “virus sterilizing techniques” and the use of “artificial factors” have greatly reduced this risk. Hemophilia A can also be known as classic Hemophilia (because it is more common) and factor VIII deficiency. Hemophilia B is also known as Christmas disease, and factor IX deficiency.
Haemophilia is used to describe a collection of hereditary genetic diseases that affect a mammal’s body’s capability to control thrombogenesis. Thrombogenesis is the way in which blood clots which is an important role in haemostasis. Two common forms of haemophilia are A and B. (1) Someone with A (otherwise known as classic haemophilia), clotting factor VIII is does not exist enough or is entirely absent. A person with haemophilia B (otherwise known as Christmas disease), clotting factor does not exist enough or is also entirely absent. Those with the disorder do not bleed a lot they just simply bleed for a longer period of time. All people with haemophilia A or B are born with the disorder as it is a hereditary disorder and passed down through generations very few cases of haemophilia are not genetic and are therefore rendered a spontaneous gene mutation which is then passed down.
Hemophillia is a rare bleeding disorder in which the blood does not clot normally. Hemophillia is usually inherited and people born with it have little or no clotting factor (a protein needed for normal blood clotting). These proteins work together with platelets to help the blood clot. When blood vessels are injured, clotting factors help platelets stick together to plug cuts and breaks on the vessels. Hemophillia usually occurs in males with about 1 in every 5 000 males being born with the disease each year. A hemophiliac does not bleed more intensely than a person without it but can bleed for a much longer time. In some severe cases, continuous bleeding occurs after minor trauma or can even happen spontaneously.They may also bleed inside their body(internally), especially in the knees, ankles, and elbows. The bleeding can damage organs and tissues and may be life threatening. There are two main types of hemophilia: A and B. People born with type A are missing or have low levels of clotting factor VIII (1 in 5 000 males). People born with type B are missing or have low levels of clotting factor IX (1 in 20 000 males). About 8 out of 10 people who have hemophillia have type A. The greatest concern for both types is deep internal bleeding and bleeding into joints. Hemophilia is a life long disease, but with proper treatment and self-care, most people maintain an active productive lifestyle.
Tsar Nicholas II and his Tsarina, Empress Alexandra, had only one son, Tsarevich Alexei. However, Alexei had inherited from his great-grandmother Queen Victoria the life-threatening genetic disease hemophilia B, a sex-linked genetic disease on the X chromosome that caused a condition of deficiency in blood-clotting and excessive bleeding, symptoms that usually remain hidden unless contracted by a male (Fuhrmann 37; King 28). To Nicholas II, it was imperative that he have a son to succeed him to secure the throne. Alexei was Nicholas’s sole male heir, giving Nicholas the incentive to protect his son at all costs. Without a scientific cure for the genetic disease, Alexandra turned to religion, namely Grigori Rasputin, a poor uneducated Siberian peasant to protect her son.
Imagine waking up one morning and having blisters all over your body and every one was the worst itch you’ve ever had. That’s what having chickenpox is like. Before there was a vaccine, chickenpox caused about 4 million people to get sick, more than 10,500 hospitalizations, and about 100 to 150 deaths each
My uncle tortured, and ended up killing my grandma. Well, not in the way you expect and not in the way you’re thinking. My grandma had fallen and broken her hip, so she was taken to the hospital. Her condition, already quite bad, rapidly deteriorated and eventually she was comatose. My uncle, distraught and worried, could not accept the fact that she was dying and decided to put her on life support. For three weeks, my grandma was stuck on life support, not quite living and not quite dead. After my uncle finally allowed the removal of life support, my grandma passed away. What I’m saying is that, my uncle could have just let nature take its course with her rather than choosing life support. I can completely understand however, why he would
By this time tomorrow, 12 people in America who are alive right now will be dead.
Kids are meant to be happy, play outside, go to school, and have fun. They aren’t meant to sit in hospitals, losing weight by the pound, carrying around IV poles filled with poison. It’s ridiculous and immature that we don’t have a cure for childhood cancer. The only “treatment” that we have is chemotherapy- a chemical that seems to help fight off cancer. Chemo doesn’t just fight off cancer cells though- it fights off healthy cells in your blood, mouth, digestive system, and hair follicles. The most frustrating thing about childhood cancer is that only 4% of federal funding is exclusively dedicated to childhood cancer research. It is true that more adults get diagnosed with cancer than kids, but does that mean that adults are 96% more important than children? The average age of diagnosis for an adult with cancer is age 67, and the average number of years lost is 15. 15 years are definitely many years, but not that many compared to the average number of years lost for a child- 71. Also, age 67 is a lot older than the average age of diagnoses for a child- age 6. At least the adults get to grow up and have the ability to even have cancer- some of these kids can’t even get through a fifth of their lives.
Transfusions of red blood cells, platelets, and plasma are critical to a patient's return to good health,
**INTRODUCTION** Hello everyone, I am here again to tell us about another flesh eating disease. The previous one I talked about was the Necrotizing Fasciitis, you can read about that one [here](https://steemit.com/steemstem/@florae/necrotizing-fasciitis-the-flesh-eating-disease-it-s-brief-history-causes-diagnoses-prevention-treatment-mode-of-entry-etc) its a deadly one too and also has similar features with the one I’ll identify in this article. Ladies and gentlemen allow me to introduce you to the **Buruli Ulcer**. This disease or infection or disorder any one you could call it, is more prevalent in the tropics especially in west Africa and Australia.
Have you ever wondered which diseases affects the reproductive system? Today, I will be telling you one of many diseases it affects one being Pelvic inflammatory disease. Pelvic inflammatory disease is an acute infection of a females reproductive organs. It causes inflammation to your organs. Pelvic inflammatory disease (PID) is a clinical syndrome that can result from microorganisms from the vagina to the upper genital tract.