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Essay on therapies in hemophilia
Essay on therapies in hemophilia
Essay on therapies in hemophilia
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Did you know that hemophilia A is mostly common to men and happens to about 1 in 5,000-10,000 men at birth ? Hemophilia is a bleeding disorder with many hardships of their life.
Hemophilia is a Dangerous disease .
Most people who have Hemophilia are male, their blood starts to clot which make their bone bleed. People with Hemophilia tend to bleed a lot because it clots and your joints start to bleed. It is hard to walk if you have it on your knee and it’s hard to move your elbow or anyplace on your joints because with Hemophilia you tend to bleed internally. Hemophilia is a hard disorder to live with, Hemophilia you can die from it because if your blood clots you will bleed to death. It affects your joints your bones, mostly men have
it. I don’t think there are levels to Hemophilia but there are two types of Hemophilia. Hemophilia A and Hemophilia B. Hemophilia is hard to live with but with the medicine people with hemophilia can live a normal life. One step to healing hemophilia is you need to go to a replacement therapy, but that just one step of healing it. There are treatments for this disorder, but there are two types and those two types are hemophilia and Hemophilia B which need different treatments. The treatment for Hemophilia A is the clotting factor X||| and for Hemophilia B is clotting factor X|. Many people who have hemophilia, don't not have anything wrong with their but I'm pretty sure that people with hemophilia can eat normal and there nothing wrong with their mouth or stomach or anything to do with their digestive system and just part of their body are swollen With medicine they’ll be fine they’ll be back to normal there are challenges but they don’t have to overcome the challenge because there a treatment. In conclusion, hemophilia is hard to live life every day having pain your joints bleeding you can’t even walk. You could die anytime you can’t live a normal life, but with all these technologies and medicine more and more people with Hemophilia can live a normal life.
Sex-linked disorders only affect males and are passed down through female carriers. A boy inherits the disorder when he receives an X chromosome with a mutated dystrophin gene (the genetic cause) from his mother. The dystrophin gene is the largest gene found in nature and was identified through a positional cloning approach. It's a highly complex gene, a large rod-like cytoskeletal protein which is found at the inner surface of muscle fibers. (www.ncbi.nlm.nih.gov)
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.
Marfans occurs evenly in men and women and can be inherited from just one parent. Marfan syndrome is also referred to as...
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 is known about who has a bleeding disorder.... ...
Turner’s syndrome is a genetic conditions that affects the female’s sex chromosome. In (http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001417/) Turner’s syndrome occurs when cells are missing all or part of an X chromosome. It’s common of the female patient to only have one X chromosome. Although, some individuals may have two X chromosomes but one is defective. It is thought that an estimated 1 out of 2000-2500 females suffer from this genetic condition worldwide but it’s usually females with this condition don’t survive their birth. Due to this abnormality, the genes that is defective “affect the growth and sexual development of the female” (http://learn.genetics.utah.edu/content/disorders/whataregd/turner/). However other disabilities and delays do occur even though these traits can vary case by case.
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.
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.
Hemophilia is a genetic disorder in which the blood does not clot normally. It’s a rare bleeding disorder that has been happening since ancient times. Men are the ones mainly affected by it. One in five thousand men born each year have Hemophilia. Yet women can be carriers and just like men, they can suffer from symptoms too. Women can only have Hemophilia if their father does and mother is a carrier, it’s uncommon but can happen. Hemophilia affects all races and ethnic groups. It’s all based on your family tree. A man with Hemophilia will pass the gene down to his daughters, leading to them becoming carriers. A woman with the gene has a fifty percent chance of passing the gene down on to her sons. If there was no family history of Hemophilia but the woman is a carrier, a son could possibly be the first one in the family to have it. If there’s one thing for certain about hemophilia is that it does not discriminate against anyone. Hemophilia has affected royalty as well as high and low class men all throughout history.
Over one million Americans in the United States are living with or have been diagnosed with leukemia. That’s a big amount of people. I chose to do my research paper on leukemia because two years ago I lost my grandma to the cancer. I wanted to know more about the disease and what was happening to her. I researched the different types, risk factors, symptoms, treatment, and what kind of research is being done to help cure leukemia. Leukemia is a cancer of the blood cells that start in the bone marrow. During leukemia the bone marrow starts to make a lot of abnormal white blood cells or “leukemia cells”.
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.
ALL is more common in white children compared to African-American and Asian-American children. It is also more common in boys than it is in girls. AML occurs almost equally in boys and girls of all races.
Have you ever given blood? Have you ever been asked what type of blood you have? There are four different blood types, and it is very important to know which kind you have for medical reasons and for the benefit of others.
There’s to major forms of hemophilia much more communing to in occur in males then females, hemophilia A is much more common ,1 in 4000 to 1 in 5000 males worldwide is born w. this condition. Hemophilia B appixmately in 1 to 20,000 newborn males worldwide. (U.S. National Library of Medicine, 2012)Although the numbers may .seem rare it is still an extreme serious condition not to be taken lightly.
CDD is an uncommon condition. Since Heller's original description in 1908, there have been approximately 100 reported cases in literature (Volkmar, 2005). In case by case studies, the prevalence has shown to have about an equal sex ratio, although more recent studies have shown that CDD is slightly more common in males (Barber National Institute, 2013).