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Essay on therapies in hemophilia
Essay on therapies in hemophilia
Essay on therapies in hemophilia
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My disorder is Hemophilia, and this is a disease in which your blood doesn't clot easily. There is no cause to "get"
Hemophilia, because it can only be inherited. If there would be any cause it would be that you bleed. Symptoms of this disorder is that if you get a minor cut or scrape your knee, you will bleed uncontrollably. Kristy Dobson, who says she has Hemophilia, claims that if you injure your head in any way, there will be a major effect.
To see if you have this this disease you have to take a blood test and have a medical history discussion with your doctor.
This disorder/disease, can be treated by your doctor with a per scripted hormone. They also inject desmopressin into your vein. Noting else really contributes to my disorder other
1. This was a bad mistake. I was born with neutropenia, a blood disease that affects the
Originally thought to be an obscure illness, it was later identified as the most common genetic disorder for those with a Western European background. However, due to its low penetrance rate, only one out of two hundred are said to have the condition. Hemochromatosis is treated by the practice of bloodletting. It is one of the oldest treatments recorded in history, with its earliest records dating as far back as 3000 years ago in ancient Egypt. Routinely bleeding is beneficial as it not only reduces the iron in the bloodstream, but also combats issues such as heart disease and high blood
There is also counseling, with peer support, and support groups this can be very helpful. There are 3 support groups I found, National Adrenal Diseases Foundation, The MAGIC foundation, and the CARES foundation. All of them are focused to improve the lives of individuals with this disease.
There is no actual treatment or any pharmaceutical cure for facioscapulohumeral muscular dystrophy. The only way to cope with this disorder is to treat the side effects it causes and prevent any other complications that arise from the onset of facioscapulohumeral muscular dystrophy.
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 anywhere in the body. People with hemophilia bleed longer, not faster.
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.
For some types of MD, medication can help. Guys with Duchenne MD may be helped by a medicine called prednisone, and teens with myotonic MD might use mexilitine to relax muscles.
Campos and colleagues believed that there is no cure or treatment for CPM nor is there any definitive therapy (Campos et al. 2011). However, there are medications and even vitamins that have been supportive treatments for patients with CPM. The supportive treatments include cortical hormone vitamins and even serum replacement but their exact roles remain unknown. Less than a year after determining that there was no cure or...
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.
Ways to know you have the disease is full body pain, abnormal cramps, frequent bowel movement, diarrhea, vomiting, rashes or blemishes on skin, cloudiness in cornea, decreased sweating, fever, and loss of appetite. Knowing that you have this illness takes a lot of determination. You have to monitor, manage, evaluate, and treat the disease. Testing available for Fabry disease is enzyme assay, it measures the amount of alpha GAL enzyme act in the blood. For females enzyme assay may not be as useful as genetic testing. Female screening is not simple. The blood test can be misleading because of the random X-inactivation. The GAL gene is more accurate tha...
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.
Most often there will be no signs of the disease until it is advanced in stage. But when symptoms do occur, they may be:
...urces for other interventions outside of the medical model that have proven to be effective in children with this disorder.
Symptoms will vary according to the individual. However, the disease is characterized by common symptoms: