Reye Syndrome
Reye Syndrome is an extremely rare, non-contagious disease thought to be triggered by aspirin use. The actual origin of the disease is unknown. Reye's
Syndrome, occasionally called Reye-Jacobsen's Syndrome, is known to follow any viral infection. Two of the most common viral infections it precedes is influenza, “the flu”, and chicken pox. A now-familiar warning on bottles of aspirin, most notably Tylenol, is not to give Tylenol to a child who is recovering from the chicken pox, a fever, or any other viral infection. The link between aspirin and Reye's Syndrome and is not fully understood, but all reported cases of Reye's Syndrome include a child who has received aspirin before infection.
Symptoms of Reye's Syndrome may often be mistook for a recurrence of the flu, or extreme exhaustion. These symptoms include vomiting, confusion, lack of coordination, distorted balance, irritability, a stupor-like state, and a recent infection from a viral illness. The symptoms often begin with vomiting and progress to a stupor and near comatose state. This disease is often found in young children and infants. Over sixty percent of reported Reye's Syndrome cases occur in children under the age of sixteen, with the majority of these cases being in children under six. Although less than five percent of Reye's
Syndrome cases occur in people over the age of sixty, the elderly are often the most severely affected, due to old age and weakening immune systems. Infants, while hindered by their young age, can often fight the infections of Reye
Syndrome better, for reasons doctors do not yet fully understand. The severity of Reye's Syndrome is classified on a scale of 1-5, with one and two being the onset of symptoms and four and five being the most severe, with the patient being comatose. With the most severe of Reye's Syndrome cases, internal fluid builds up in the brain and there is irreversible brain damage or even death.
While the disease is not often fatal, it is essential to treat the disease early.
Reye's Syndrome is not contagious, but the diseases that can lead to, such as the flu, and chicken pox, are highly communicable.
The first case of Reye's Syndrome was diagnosed in 1963. Looking back into medical journals, there were many “mystery illnesses” that had the same symptoms as Reye's Syndrome, but no cases were positively diagnosed as being
Reye Syndrome until this date. The definitive tests for this disease are a liver biopsy and blood analysis. The liver biopsy can help determine the presence of fat and lipid formation in the liver. Upon surgical examination, the liver is slightly enlarged, firm, and bright yellow.
On July 27th, 2015 a young woman named Maylin Reynoso went missing. She was last seen leaving her job at a gas station and after this her friends and family went to social media to ask people if they had any information about where Maylin could be. Other than these posts on Instagram, Tumbler, and Facebook there was no news coverage about her disappearance. Sadly, Maylin’s body was found three day later in the Harlem River, she was only 20 years old; although she had been found dead there was still no news coverage about her (Blay, 2016). The worst part of her death was that her family did not know about her body being found until a week later. The family was only able to identify Maylin’s body because of her tattoos. During that same week
...oms that come along with it. There is a possibility that the disease will be transmitted to the offspring of the infected person. Having a splenectmomy conducted will not cure the disease it will only make it go into remission.
in the first place and was suffering from other major illnesses. The society does not
Sirenomelia What are the other names for this condition? also known as synonyms. • Mermaid Syndrome • Sirenomelia Sequence • Midline Disorder • Sirenomelus What is the 'Standard'?
One very special case can be displayed by none other than David Beckham, the famous international football star. He says that he has tried various treatments, but the biggest success came from learning to live with the disease (Healthguru, n.d.). His family is also very supportive of his condition, which shows how important family support is. Quoted by Victoria Beckham, his wife, “We've got three fridges - food in one, salad in another and drinks in the third. In the drinks one, everything is symmetrical. If there's three cans, he'll throw one away because it has to be an even number” (Frith,
...se it eventually kills. I learned about Lupus from my mother who struggles to be healthy on a daily basis and also from my aunt who thought she was dying from Liver failure, but it was the Lupus that eventually killed her. I only hope that you have come to understand Lupus and the unpredictable nature that accompanies it.
Cardiofaciocutaneous syndrome may be generated through various genetic mutations. As mentioned before, there are four genes that can cause this condition to be brought about in an individual. The most frequent mutation of these is the BRAF gene, because it is responsible for approximately 75 to 80 percent of each case of the syndrome. The two genes, MEK1 and MEK2, are very much alike and together are the result of 10 to 15 percent of ...
Girls with this syndrome may have many middle ear infections during childhood; if not treated, these chronic infections could cause hearing loss. Up to the age of about 2 years, growth in height is approximately normal, but then it lags behind that of other girls. Greatly reduced growth in height of a female child should lead to a chromosome test if no diagnosis has already been made. Early diagnosis is very importance in order to be able to give enough correct information to the parents, and gradually to the child herself, so that she has the best possibilities for development. Early diagnosis is also important in case surgical treatment of the congenital heart defect (seen in about 20 per cent of cases) is indicated.
...agnosed at a later stage, most people die within two years of diagnosis and treatment.
...atment option your doctor suggests, careful monitoring and follow-up visits are required to successfully combat the symptoms.
The disease has an unpredictable clinical course. This means it’s hard to give a prognosis in any single patient.
symptoms between the ages of 30 and 50, but has been known to show itself in
Rogers, R., Salekin, R. T., & Sewell, K. W. (1999). Validation of the Millon Clinical Multiaxial Inventory for Axis II disorders: Does it meet the Daubert standard?. Law And Human Behavior, 23(4), 425-443. doi:10.1023/A:1022360031491
The purpose of this paper is to analyze, diagnose, and to determine a proper treatment plan to work toward the beneficial prognosis for the individual indicated within the case study.
“Prevention is better than cure” preventing risk at the early stage is better than planning for it when it happens. There are several risk management tools such as Cause and Effect diagram, Fishbone