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❶Down Syndrome Down syndrome is a genetic disorder in which person have 47 chromosomes instead of the usual Marfan syndrome is caused by a defect or mutation in the gene that tells the body how to make fibrillin

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An American Literature Research Paper: How to Create One. Down Syndrome Research Papers: Research Papers on Movies: What Is Your Favorite One? Employment Privacy Policy Terms and Conditions. Services provided by Writing-Services. Additional research activities are described below. The project aims to understand critical health and quality-of-life needs for individuals with Down syndrome, with the aim of yielding scientific discoveries to improve the health, well-being, and neurodevelopment of individuals with Down syndrome, as well as their risk and resilience common diseases that they share with individuals who do not have Down syndrome.

Since , the Institute has led the Down Syndrome Consortium , a public-private collaboration that provides a forum for promoting the Down Syndrome Directions: NIH Research Plan on Down Syndrome and fosters the exchange of information on biomedical and biobehavioral research on the syndrome.

Consortium members, who represent public and private organizations, work to avoid duplication of research efforts and to inform the Down syndrome community of research advances. Creation of this registry was one of the principal recommendations of the Down Syndrome Research Plan. The Down Syndrome Registry? The Down Syndrome Registry text alternative. A key focus for the IDDB is exploring treatments for Down syndrome, including agents that improve intellectual development and cognitive performance.

Because of similarities between certain mouse and human chromosomes, mouse models have allowed significant advances in understanding potential treatments for Down syndrome.

Using a mouse model for Down syndrome, NICHD researchers showed that by administering neuroprotective peptides small protein sub units to mice before birth, they perform better on memory and learning tasks as adults. The peptides, NAP and SAL, are sub units of two proteins that are important in brain development because they enhance the ability of brain cells to receive and transmit signals, and enable them to survive. Mice with the extra chromosomal material that were treated with NAP and SAL in the womb learned as well as mice that did not have the extra chromosome and significantly faster than mice with the extra chromosome that were treated with saline solution placebo.

In an earlier study, NICHD researchers showed that when mice with the extra copy of chromosome 16 were treated with NAP and SAL in the womb, they achieved developmental milestones earlier than did untreated mice. In this earlier study, the researchers examined developmental milestones for sensory, motor skill, and muscle tone in the first three weeks of life.

Together these study findings show that NAP and SAL treatments improve both physical development and learning ability in a mouse model for Down syndrome. Other research focuses on the causes and pathophysiology of Down syndrome.

It is also called as 11q terminal deletion disorder. Symptoms of dis disease are wide set eyes, small lower jaw, small lower jaw, broad nasal bridge etc. Other Characteristics of Jacobsen syndrome can include heart defects, feeding difficulties in infancy , short stature, repeated ear and sinus infections, and skeletal abnormalities.

Jacobsen syndrome can also affect the digestive system , kidneys , and genitalia. Currently there is no specific treatment for Jacobsen syndrome. Turner syndrome is a chromosomal condition that effects development in females.

It is also called as Monosomy X. Turner syndrome is related to X chromosome; normally females have two X chromosomes.

The symptoms of this disease are High blood pressure , kidney problems, skeletal abnormalities , short stature, Heart problems etc. It is also called as 5p syndrome. Cri du chat syndrome is a rare genetic condition caused by the deletion of genetic material on the small arm of chromosome 5. This syndrome makes infants produce high pitched cry similar to cat. This disease categorized by intellectual disability, small head size, low birth weight, weak muscle tone in infancy.

The symptoms of this disease are small head size, widely-space eyes, small chin, and Small nose, Respiratory problems etc. Prader-Willi syndrome is a disorder caused by loss of genetic material from proximal arm of chromosome An important characteristic of Prader-Willi syndrome is a continuous sense of hunger that usually begins at around 2 years of age.

Persons with Prader-Willi syndrome want to eat constantly because they never feel full hyperphagia and usually have trouble controlling their weight. Many problems of Prader-Willi syndrome are due to obesity. The common features of this disease are mental retardation, short stature , small hands and small feet etc. Please leave a message, we will get back you shortly. Home Publications Conferences Register Contact. Guidelines Upcoming Special Issues.

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Down Syndrome Research Paper Down syndrome is a chromosomal condition in which an individual possesses extra genetic material, specifically an extra complete or partial duplicate of chromosome 21 in some or all of an individuals cells.

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Down Syndrome research papers discuss this genetically based mental handicap. This is a topic suggestion on Down Syndrome from Paper Masters. Use this topic or order a custom research paper, written exactly how you need it to be.

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