Usher Syndrome Research Paper

Humans are often fascinated and petrified by the supernatural. This is because the supernatural has the ability to hurt us humans in ways we cannot avoid. As a result, people start thinking how all of this is possible. Supernatural beings are often very peculiar, so, not only are their actions frightful, but so too are their appearances. Many horror writers take advantage of the supernatural, as Edgar Allan Poe did. In Poe’s short story “The Fall of the House of Usher,” the characters have a rare illness that has the same symptoms as a vampire would. Poe does not state if the characters are vampires, so there are many debates as to whether they have an illness or if they are vampires. It is evident that the characters are actually vampires based upon Roderick’s symptoms and looks.

Romanticism was a noteworthy global development that was compelling in forming present-day perspectives of artistry, writing, and music. Be that as it may, it came later in a few nations, for example, Italy, Spain, and the United States. It happened first in craftsmanship and writing and later in music. To a limited extent, sentimentalism was a response to the creative styles of traditional vestige. These styles had been resuscitated in the 1600's and 1700's as neoclassicism. Neoclassicists set remarkable significance on the force of reason as a method for finding truth. That is the reason the neoclassical period is frequently called the Age of Reason (Wheatley, K.).

The National Human Genome Research Institute (NHGRI) and the National Coalition for Health Professional Education in Genetics (NCHPEG) have expressed the need for the education of physicians about the ethical, legal and social implications (ELSI) related to Lynch Syndrome assessment, genetic testing and counseling (Metcalf, Tanner, Buchanan, 2010). To address this need, a local medical organization has called upon a health consultant and educator to conduct an educational assessment and training on Lynch Syndrome for primary care physicians and other healthcare professionals in their organization.

There are many different types of syndromes and disease in the world today. Steven Johnson is one of them. This Syndrome is a very rare disorder in the world today. Many persons do not have a clue in which what this serious is or/and why it occurs. The Steven Johnson syndrome is a disorder of someone’s skin or mucous infection. This occurs when the persons take medication(s) that they are possibly is allergic to. It’s really not the medication but it’s like the medication is fighting off some good cells in the body. Steven Johnson Syndrome is a very serious syndrome or infection. It requires hospitalization and serious care.

Sweet syndrome is a rare disorder characterized by fever and the sudden onset of a rash, which consists of multiple tender, red or bluish-red bumps or lesions. These lesions usually occur on the arms, legs, trunk, face or neck. In some cases, additional systems of the body can become involved including the musculoskeletal system such as inflammation of the joints (arthritis), the eyes such as inflammation of the conjunctiva or the membrane that lines the eyes (conjunctivitis), and the internal organs.

The prevalence of hearing loss has doubled over the past 30 years in the United States and continues to steadily incline as time goes on. Hearing loss itself encompasses a wide variety of disorders, effects many diverse populations, and is caused due to a multitude of different sources (“The Prevalence”). Its onset is also extremely variant and could happen either congenitally or at any point later on in a person’s life. One of these such congenital disorders is Waardenburg syndrome. Waardenburg syndrome is a genetic disorder characteristized by four different types of specific disorders that are further differentiated by their physical attributes and genetic causes. It’s estimated that about 1 in 40000 people are diagnosed with this disorder

Usher syndrome, is also known as Hallgren syndrome it is one of the most common disorders that effect your hearing and vision. Hearing loss and a condition called retinitis which is an eye disorder are the two major symptoms of this syndrome. RP means a chronic hereditary eye disease characterized by black pigmentation and gradual degeneration of the retina. Night blindness and loss of peripheral vision are caused by the degeneration of the retina due to RP. A mutation on the USH2A gene is known to cause 10% to 15% of a syndromic form of RP.

Usher syndrome is an inherited syndrome and is presented in someone with difficulties with both hearing and vision. The symptoms are hearing impairment and retinitis pigmentosa. Retinitis pigmentosa causes for the vision to deteriorate over time. There are also three types of Usher syndrome: Type 1- the individuals are profoundly deaf at birth and they will have difficulties with their balance. They vision problems develop around the age of ten. Type 2- they are born with moderate to severe hearing loss and has normal balance. They mainly perform well in school and can benefit from hearing aids. Their visual problems happen at a slower rate than someone with type 1. They can get blind spots, but they appear when they enter adolescence and then

Turner Syndrome is a genetic disorder that effects a girl’s development. Girls who have it are short, and most are infertile. Girls and women that have turner syndrome are at a risk for many health problems, including high blood pressure, kidney problems and diabetes. There is no cure. But treatment can help reduce symptoms as you read in the text below. This information stated below will explain health issues of turner syndrome. It will also cover symptoms and causes of this disease as well as diagnosis and treatment options.

What Color Blindness and Usher Syndrome have in common is that they both affect the eye. They both change the way the person sees by blindness or color alteration. The difference between the 2 disorders is the mode of inheritance. Color Blindness is X-linked recessive; That means the disorder is carried on the X chromosome. Usher Syndrome is autosomal recessive, which means the disorder is carried on any of the 22 chromosomes. The disorder is carried on 10,12,13,15,18 or the 20th chromosome.

The Mucopolysaccharide disease or also known as Hunter Syndrome is an inherited condition and it is a rare inborn of metabolism characterized by inadequate production of an enzyme known as iduronate sulfatase, which is needed to break down complex sugars that produced in the body. This disease usually involves males. And the severe form of the disease starts at the age of 2.

They only hang out in Darling basement because both Aunt Fee and Kojo are always working in the afternoon. They mostly just watch pornography in the basement. They have been watching them in alphabetical order. Darling is interrupted by a call from Africa, it’s her Mother. Mother lectures Darling for not calling her. Darling talks to her friends from Africa. They end up bombarding her with questions about America. She gets startled when they ask her when she is going to visit them. She gets saved from the call when a package gets there. She says she’ll call back but never does. When it gets back to the basement they had gone and watched without her. Marina ends up bringing up a link of a cool video. They press play and it shows the warning of this film contains some disturbing images. The video starts off with a girl forced down by other women while one is a knife wielder. The video continues with the girl screaming, crying, and begging them to stop. Marina is unable to bear watching it and runs out. They skip near the end where the girl is quietly in a corner and bloody. They're never going to speak of this again.

Lynch Syndrome is genetically heterogeneous, autosomal, and dominant. Nearly all patients contain a mutation in one of the subsequent four DNA mismatch repair genes: MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), MutS homolog 6 (MSH6), or PMS1 Homolog 2 (PMS2). 3 In atypical cases, the deletion of the 3’ end of epithelial cellular adhesion molecule gene (EPCAM), located upstream of MSH2, results in epigenetic hypermethylation of the MSH2 promoter resulting in Lynch Syndrome. 2 Figure 1 is a fabricated example of a familial pedigree that contains an autosomal dominant disorder such a Lynch Syndrome.

Marshall’s Syndrome is a rare autosomal dominant genetic disorder. It causes distinctive facial features and limits hearing, smell, and sight based senses. It is caused by irregularities in the COL11A1 gene. Research on the disease is limited. The number of people affected by it is unknown due to little research on the subject. Though the disease causes many problems for the people affected by it, it’s not impossible to live a normal life while suffering from its effects.

Kleinfelter’s Syndrome is a syndrome that I find interesting. This syndrome affects males and is usually not diagnosed until around the age of puberty. In order to reach a diagnosis, a doctor may do a physical exam, get a health history and perform a karyotype. Kleinfelter’s syndrome occurs with the presence of extra X chromosomes in males. The extra X occurs when the egg or sperm splits unevenly. Even though this is considered a genetic syndrome, because of how it occurs, it cannot be passed on. There are three different ways that Kleinfelter’s may present.