The author concludes with his own story, about a mysterious neuromuscular disease that is gradually robbing him of his mobility. Like the prion diseases, his is a disorder of misfolded proteins. However he realizes that his condition is not as fatal as familial insomnia or the other destructive prion diseases. Ultimately, I believe that D.T Maz presents the mysterious past and possible future circumstances of medical diseases. The more we research and analyze these cases, the better interpretation we can have towards a…
Review the following two case studies. Each patient is being referred to a specialist for further evaluation of a nervous system disorder. Outline characteristics of the disease each patient is suffering from by answering the questions associated with each case study. Answer in your own words.…
Caritas Pirckheimer, held the position of an abbess in her convent, and encountered religious conflicts during her time in Nuremberg, Germany, St. Claire church. Between the years of 1524 to 1528, the Reformation created an issue where Pirckheimer, defended her cloister and sisters' rights in the City council's attempt to close it down and force the members to renounce their vows. The council made an effort to replace the Franciscans, who had been preachers and confessors to St. Claire, with different preachers who advocated the doctrine of Lutheranism (68). These efforts turned out to be problematic because the teachings of the Lutherans preached Christian freedom, and the idea that the laws of the Church and oaths of religious orders were invalid, and no one was obligated to keep them (68). The Protestant Reformation was a period where numerous convents had lost their spiritual focus because of the Lutheran preaching's. Some women were placed in convents against their will because of their families not being able to afford the high marriage dowries (Wiesner, 211). Therefore, many nuns took advantage of this freedom and "threw of their robes and habits" (68), wore secular clothing and jewellery, entertained visitors, ate fancy food, and left the convent to visit their family and friend (Wiesner, 210). The reformation sought to close the monasteries through persuasion, political pressure and physical intervention by townspeople and peasants (67).…
Alzhaimer`s disease-around 500.000 people in the UK have Alzhaimer`s.Scientists know that during Alzhaimer`s two abnormal proteins build in the brain. They form clumps called either "plagues" or "tangles". Theses plagues and tangles interfere with how brain cells work and communicate wih each other. The plagues are usually first seen in the area of the brain that makes new memories.…
Dave Pelzer was born on December 29, 1960 in Daly City, California. He is the son of Stephen Pelzer, who was of Austrian and Irish descent, and Catherine Pelzer. Dave Pelzer was the second of five boys in the family. He has experienced a truly horrific lifestyle. As a child, he endured the horrors of child abuse, this included physical torture, mental cruelty, and was nearly starved to death. His mother referred to him as “it”, he was the only child that was abused. The rest of his brothers lived a happy typical life. Dave, on the other hand, was looked at as the family slave. He was forced to sleep in the cold, dark basement on a cot with no blankets or pillow. He had only one pair of clothes and they were all torn and worn out from over the years. It all started when Dave was about two years old.…
In contrast to Beatty, Montage is a character who went through from a literary darkness to self-enlightenment. At first, Montage was ignorant as shown that he enjoyed burning books. But as he met Clarisse, his curiosity has led him to question things in ways he has never done before. Clarisse sparked his curiosity to question things when she asked him whether he was happy. Later on, he was confronted by knowledge as he sees the old lady willing to sacrifice for books. This has led him to reflect on their importance. Montage was eventually determined to gain more knowledge and find greater significance in his life. “Do you know why books such as this are so important? Because they have quality. And what does the word quality mean? To me it means…
Kety supports Gottesman in the role of genes in the development of sz. He conducted a study with 207 offspring of mothers diagnosed with sz which he called the high risk group, along with a matched control of 104 children with healthy mothers. The children were between the ages of 10 to 18 years. Sz was diagnosed in 16.2% in high risk group compared with 1.9% in low risk group. Erlenmeyer-Kimling conducted a follow up study 25 years later.…
Progeria, otherwise known as Hutchinson-Gilford syndrome is an extremely rare, generic childhood disorder with reported incidence of about one in a million. Hutchinson has reported the syndrome in 1886 when he found the first patient with Progeria. In 1904 Gilford described a second case of Progeria, thus creating the term to reflect the syndrome 's senile features. There are only about a hundred reported cases since the disorder has been discovered over a century ago. Currently, there are about thirty to forty known cases worldwide of Progeria. Affected children age up to seven times faster, have "plucked bird" appearance, many health problems and their lifespan is about thirteen years. There is neither known cause nor cure for this disease. It is usually first diagnosed based only on appearance and treatment is given for other conditions associated with the aging process rather the disease it self.…
Mermann, A. (1992). Yale Journal of Biology and Medicine. New Haven: Yale J Biol Med.. p137-142.…
Tay-Sachs disease is an autosomal recessive disease that affects the lysosome storage in cells. Over time, the disease deteriorates the functions of the body leading to blindness, deafness, dementia, and recurrent convulsions in the terminal stages. Unfortunately, its main victims are children, who often show the first signs and symptoms at around 6 months old and usually do not live past the age of 5. There is also a juvenile and late-onset form that may not appear until the second or third decade of life. By the year 1993 (American Medical Association), geneticists were able to identify that the cause of this disease is triggered by a mutation in the HEXA gene, located at 15q23-q24, which codes for the hexosaminidase A enzyme. Without this…
Because the jury issues but a mere advisory opinion and not binding upon the court, Florida’s sentencing scheme must be unconstitutional. Florida’s statute requires that a court imposing the death sentence must make a written, detailed finding. This detailed account—not the jury’s verdict—that furnishes the basis for the Supreme Court of Florida’s review. Respondent’s rely on Hildwin (1989 case that permits the judge to find aggravating circumstances that authorize the death sentence) because it has not been expressly overruled. The ideas and principles in Hildwin were thrown out with Walton, clarified in Ring, and expressly overrule today.…
MS is far more common in countries with temperate climates, including Europe, southern Canada, northern United States, New Zealand and southeastern Australia. The risk seems to increase with latitude and affects noticeably more women than men with the onset of clinical symptoms occurring between 15 and 50 years of age. It is the most common demyelization disease of the central nervous system. In the United States alone, there are at least 250,000 cases. Although the exact pathogenesis of the disease is unknown, it is believed that the clinical manifestations of multiple sclerosis are the result of an immune reaction consisting of the penetration of the blood-brain barrier (BBB), entrance into the CNS, and recognition of the myelin basic protein (MBP) and proteolipid (PLP) as foreign. The immune system 's attack on these proteins induces the stripping of the protective coating of myelin and then eventual formation of plaques. These plaques or lesions can be found throughout the central nervous system, but are most prominently found in the white matter, optic nerve, brainstem,…
Multiple Sclerosis is mainly an inflammatory disorder of the brain and spinal cord in which central lymphocytic permeation leads to harm of the myelin scabbard and axons. Initially, inflammation is temporary and re-myelination occurs but is not long-lasting. Hence, the early course of disease is characterized by occurrences of neurological dysfunction that usually recover. However, over time the pathological alterations start to take over by widespread microglia activation associated with broad and constant neuro-degeneration, the clinical correlate of which is progressive growth of disability. Para-clinical investigations show abnormalities that specify the distribution of inflammatory lesions and axonal loss (MRI); hindrance of transmission in previously myelinated pathways (evoked electrophysiological potentials); and intrathecal combination of oligoclonal antibody (examination by lumbar puncture of the cerebral fluid). Multiple sclerosis is triggered by ecological dynamics in individuals with multifarious genetic-risk profiles. Licensed disease modifying agents lessen the rate of recurrence of new episodes, but do not repeal fixed insufficiencies and have questionable outcomes on the long-term accumulation of disability and disease development. They foresee that future studies in Multiple sclerosis will provide a new classification on the center of mechanisms rather than clinical empiricism, and so enlighten strategies of improved treatment at all stages of the disease.…
Amyotrophic Lateral Sclerosis (ALS) or Lou Gherig’s is a neuromuscular disease, being that it affects the nerves and the muscles. It damages motor neurons in the spine and some in the brain. ALS is considered hereditary but is not in all cases. 90% of patients suffer from SALS, or sporadic ALS and is not hereditary directly. Approximately 10% of patients are diagnosed with familial ALS (FALS) which is passed down from parents. Family history is used to distinguish between the two, if one or more person had ALS, or troubles with speech or walking, it is more likely to have FALS than SALS. FALS can be inherited in more than three ways; autosomal dominant, autosomal recessive or X-linked. Autosomal dominant is when the person affected…
Giovanni Battista Piranesi and his writings exerted a huge influence on many contemporary and later designers and architects. Briefly outline Piranesi’s main works and account for the effect they had on others.…