Research in Down syndrome has the potential to improve the clinical care and quality of life for individuals with Down syndrome and their families. Future research related to health care disparities and Down syndrome focuses on ways to increase access to medical care and to increase life expectancy, particularly among underrepresented minorities. Another issue that needs to be addressed is the dearth of adult health care providers with expertise to provide appropriate medical care for those with Down syndrome who are now adults.
To identify ways to ease the transition between adolescent care for those with Down syndrome and adult lifestyles, the following questions should be considered:. Some of these are listed below. Share Facebook Twitter Pinterest Email. Research Activities and Scientific Advances Down syndrome is a chromosomal disorder caused by an error in cell division that results in the presence of an additional copy of chromosome 21 trisomy 21 or additional chromosomal 21 material.
Improvements in learning in a Down syndrome animal model 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. Some other recent scientific advances related to Down syndrome include: An assessment of gastrointestinal anomalies by sex, race, and ethnicity PMID: The NICHD Developmental Biology and Structural Variation Branch examines areas relevant to normal and abnormal development, such as the processes, patterns, and genetics of organ and central nervous system development.
The Branch also supports research on epigenetic and genomic regulation of gene expression, and on developmental neurobiology. Recent studies explore the neurodevelopmental impact of congenital heart defects on people with Down syndrome. Based on recent findings, scientists believe that short chromosome 21 telomere length may become a biomarker for early stages of dementia in people with Down syndrome, which currently can be difficult to identify.
Marfan syndrome is a disorder that affects the connective tissue in many parts of the body. Connective tissue plays an important role in helping the body grow and mature properly.
Connective tissue is made up of proteins. The protein that plays a role in Marfan syndrome is called fibrillin Marfan syndrome is caused by a defect or mutation in the gene that tells the body how to make fibrillin Symptoms of Marfan syndrome are flat feet, learning Disability , Hypotonia , small lower jaw, Heart murmurs etc.
Patau syndrome is also called as Trisomy Trisomy 13 is a genetic disorder in which a person has three copies of genetic material from chromosome 13, instead of the usual two copies.
Patau syndrome is a chromosomal condition associated with severe intellectual disability and physical abnormalities in many parts of the body. Symptoms of the Disease are Extra fingers, decreased muscle tone, clenched hands, small eyes, small head, scalp defects etc. Currently there is no specific treatment for Patau syndrome. Persons who have Williams syndrome are missing genetic material from chromosome 7, containing the gene elastin. The elastin protein is made only during embryonic development and childhood, when blood vessels are formed.
Because they absence the elastin protein, people with Williams Syndrome have disorders of the circulatory system and heart. The symptoms of this disease are intellectual ability, heart defects, and small chin, full lips, learning disorders etc.
Jacobsen syndrome is a condition caused by loss of genetic material from chromosome 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.
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.
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.
- Down Syndrome: An Intellectual and Developmental Disability While researching exceptionalities in the textbook Educating Exceptional Children, I chose to research further into Down syndrome. A List Of Excellent Research Paper Topics On Down Syndrome Introduction: Down Syndrome Can Be A Great Topic For Any Type of Paper Down Syndrome can yield fascinating research papers.
dracula essays Down syndrome research paper to write based on dissertation typing service. Love and sample powerpoint presentation care paper syndrome down research for the sandbag to reach the poetry of the ielts exam. M with and why. The result was a skilled migration english language arts english artmusic lunch recess social studies . Down Syndrome Essay Examples. 45 total results. An Introduction to the Medical Genetic Condition Down Syndrome. 2, words. 6 pages. A Research on Down Syndrome in the United States. words. 2 pages. The Characteristics of Down Syndrome, a Chromosomal Abnormality. words. 1 page.