An overview of the genetic neurodevelopmental disorder known as Williams syndrome.
Written in 2008; 1,748 words; 5 sources; APA; $ 56.95
Paper Summary:
The paper discusses the social behavior and social characteristics of Williams syndrome as well as the differences in the brain systems and networks. The paper looks at how individuals with Williams syndrome have specific strengths and weaknesses and notes that the study of the human brain in general may gain much from the study of this syndrome.
Outline:
Abstract
Statement of Problem
Introduction
Effect, Social Behavior and Social Characteristics of WS
Brain Differences in Individuals with WS
Major Findings
Conclusion
From the Paper:
"Williams Syndrome is a genetic neurodevelopmental disorder that is rare and is only recently being understood by science, and occurs in only one in 7,500 live births. This condition stems from a deletion, or genetic aberration which results in a missing hormone, on chromosome 7q11.23 and causes the individual to display physical and neuropsychological profile characteristics. Also included in the gene deletion is gene ELN, which is the gene responsible for coding important elastic protein, elastin, in connective tissues that are especially present in the larger blood vessels in the body such as the aorta."
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