Williams Syndrome Research Paper

From the perspective of a boy who has a brother with downs syndrome. My little brother Bryce who is 12 years old has downs syndrome, he has always been a major handful. There are advantages and disadvantages to having a brother like him. I hear lots of different opinions about people like him. It is hard to teach him how to do things. You might think it wouldn’t be that much of a difference between having a normal sibling and a special needs sibling, but there is.

Williams Syndrome(WS) is considered as a neurodevelopmental disorder, caused by a contiguous gene deletion of about 26 genes from the long arm of chromosome 7(Peoples et al., 2000). Since it had been first aware by J.C.P. Williams in 1961(Lenhoff, Wang, Greenberg & Bellugi, 1997), Williams Syndrome has drawn more attention in last 40 years. the incidence rate is approximately 1 in 2000 and diagnosed generally at 6.4 years old (Morris, Demsey, Leonard, Dilts & Blackburn, 1988). People with WS usually show a developmental delay at the early age and are affected all life long. Williams Syndrome is characterised by some abnormalities in physical, behavioural, and cognitive.

Erythema multiform: target lesion is the classic presentation, and the 3 skin manifestations are dusky center, inner pale ring, and erythematous outer border. It usually affect age 10-40y/o. Hypersensitivity reaction is most commonly triggered by infection so treat the underlying cause. HSV is most common cause so treat with acyclovir. It is a self limiting condition.

This causes delays that, to me, are similar to Down’s syndrome. Mild to severe delays can be present with this diagnosis. The OTR at my site explained that with any chromosomal defect, the delays that occur will depend on the chromosome that is affected. Just like Down’s syndrome has its own characteristics, this defect has its own characteristics too. The child that I get to treat with this diagnosis is non-verbal, she is very low tone and also has some visual and hearing impairments. She also demonstrates sensory integrations problems. She is a very pleasant eight year old and for the most part is very willing to work. It is difficult to work with a child that is non-verbal. I feel like a mind reader some days! I really have to watch her expressions to figure out if she can or wants to do something. Some of the activities I try to do, she does not want to do. I do not give her a choice; she at least has to try. When she is finished, she plops to the ground and lays down! She plants herself like she is modeling in a photo

Since Williams Syndrome is a disorder characterized by the deletion of genes, treatments for this disease are very limited. There is no cure for this disease. There is no reprieve. There is no rest from the fact that the individual’s chromosome is missing over a megabyte of data (Meyer-Lindenberg, 2004). Due to the loss of elastin in the cardiovascular system, specifically in the heart, exercise is something that can be prescribed in order to prevent the arteries, veins, and chambers from collapsing or hardening (Thompson, 2003). Exercise is important for any person to keep the cardiovascular system healthy; however, exercise is essential for a patient with Williams Syndrome (Siomou, 2014). Williams Syndrome patients often need professional

Diagnosis of Mallory-Weiss syndrome is made by your specialist amid a complete physical exam. Your specialist will get some information about any therapeutic issues, including day by day liquor admission and late sicknesses, to distinguish the fundamental reason for your side effects.

Prader-Willi syndrome (PWS) is a complex genetic disorder caused by a chromosomal abnormality. It is characterized by mild to moderate hyperphagia, severe obesity, intellectual disabilities, and behavioral and psychiatric difficulties. Characteristic behavioral disturbances in PWS include excessive interest in food, skin picking, temper tantrums, obsessive and compulsive behaviors, and mood fluctuations. It occurs in approximately one in 25,000 to 30,000 live births with no distinguishing sex or race association.

Prader-Willi syndrome is a disorder that causes you to not feel satisfied with what you eat and not feeling full. This disorder affects many parts of the body. Prader -Willi syndrome is also very rare. Most people that have Prader – Willi syndrome then you most likely have type 2 diabetes. This is also a negative mutation.

Within the couple of hours of my niece Janelle being born, doctors were concerned how little she was and her slow mobility. Unaware of her condition in Brownsville, she was sent to Driscoll Hospital in Corpus Christie within a couple of weeks. While being in the care at the hospital, medical doctors diagnosed Janelle with Prader-Willi Syndrome. As you can imagine, so many questions and thoughts went through her parent’s minds. To start, what is Prader-Willi Syndrome (PWS)? According to Genetic Home Reference, PWS is a complex genetic condition that affects many parts of the body, such as muscle tone, insatiable appetite, intellectual impairment, and learning disabilities. Which Janelle experiences these abnormalities and we have to take precautionary actions on a daily basis. It is a rare disorder present at birth and we can do nothing to prevent this and

For most families, the birth of a child with a developmental disability is an unexpected event which can often present additional challenges for parents and families. Williams Syndrome does not just impact the person who has it;

Genetic disorders offer a variety of different problems and symptoms. One of these disorders is Williams Syndrome. Williams syndrome is a genetic disorder characterized by the genetic alteration and deletion of genetic material on Chromosome 7 (Riby, 2008). This disorder can cause lack of mental functioning and have ill effects on health and other vital areas (Shiohama, 2016). Despite the drastic effects this alteration of the seventh chromosome can do, the patients that normally suffer from this disorder are socially active and have a very happy outlook on life (Lough, 2015). The purpose of this paper is to identify and describe Williams Syndrome, explain the inheritance

Genetic traits is an inherited characteristic often passed on to children from their parents from generation to generation. Some traits good, such as being smart, being tall, or being athletic. Others not so good, like cancer or sickness in the family, more specifically breast cancer in a family of woman. Cancer is a disease caused by an uncontrolled division of abnormal cells in a part of the body. No one really knows how or where cancer started, but Mrs. Terry Tempest Williams might know the cause of her family’s on going case of breast cancer. According to Terry Tempest Williams-who was part of a Mormon family that had roots in Utah-there had been a series of atomic testing in Nevada between the years of 1951 through 1962. These testing,

Turner syndrome (TS) is a disability that only affects females. The condition occurs when a female has one x chromosome instead of the usual two chromosomes. Most sufferers of Turner syndrome grow to be shorter than most children on their age group and most only have life expectancy of up to 50 years while some tragically pass away as young as 13 years old.. Although plenty of information on Turner syndrome in known, researchers and scientists are still trying to figure out exactly which genes in the x chromosome are responsible.

A child with a learning disability can be clever, and can still experience substantial cognitive complications. Learning disorders causes' brain impairment and it prevent it from processing information. A child with learning disability may face challenges as they grow; it can prevent them from studying by affecting their performances and can also affect their relationship with friends, families and colleagues.

Williams Syndrome is a genetic condition that effects about one in every ten thousand people worldwide. While William Syndrome does effect learning, there is no disconnect in social interaction. People with WS tend to be very highly social people and play strong roles in their communities as adults. Although people with WS have strengths they also have many weaknesses. Babies often have life-threatening cardiovascular problems right at birth, and on many occasions they need ongoing medical care growing up as a child. There is absolutely no treatment for WS which is what makes it so hard for them. People with William’s Syndrome can live a happy life like any of us no matter what race, gender, size, they can life just like any of us.