Williams Syndrome in Psychology Research Paper Example | Topics and Well Written Essays - 1750 words

Williams Syndrome in Psychology - Research Paper Example Yet, another similar condition can be compared with Down Syndrome, the Williams Syndrome--also known as William-Beuren Syndrome. Rare in characteristic, this type of syndrome was first recognized in the early 1960’s, where four young samples had been identified with such conditions, as all had presented â€Å"supravalvar aortic stenosis...mental retardation† and similar facial features. By such discovery, the said disorder had been named in honor of one of its founder, Dr. Williams--a cardiologist (Bellugi, Wang, & Jernigan, 1994, p. 3). Other than these initial diagnostic parameters, Williams syndrome is also characterized by hypercalcemia of unknown origin, accompanied by distinct cognitive and behavioral profile (Khan, Calureriu, Huang, & Robin, 2011). At this point, such concepts seemed to be more focused on the pathophysiological context of the said condition, disregarding the psychological elements of William syndrome. In appeal, this group is said to be hypersoci able, where they are into over-friendliness, as they appear to lack the adaptive behavior of covertly following the unwritten social rules common in most societal structures (Udwin, Davies, Howlin, & Stinton, 2007). With such social trait, one can assume that the interpersonal skills generated by individuals with William syndrome are adequate for daily public associations, yet, a number of literatures presented otherwise. The overtly sociable attitude by groups with William Syndrome may be acceptable in society, but their psychological status may not be as stable as most believed. This paper seeks to establish the paradoxical traits that individuals with Williams Syndrome seemed to have; present common psychological features and find patterns among such psychological manifestations. Biological Origins and Clinical Features The etiologic origins and pathological process seemed to be pointed back to genetic deficits. Generally thought of as a neurodevelopmental condition, most experts identified the â€Å"deletion of ~25–30 genes...(which span) about 1.5 megabases in the q11.23 region of chromosome 7† as the exact cause of the William Syndrome (Deutsch, Rosse, & Schartz, 2007, p. 903). Genetic in function, such dysfunction in the genetic level can significantly cause a series of physiological changes upon human anatomic development, especially in organ tissues of the heart. As this is genetic in origin, the defective genetic material is said to have a hereditary feature, where there can be a 50% chance that individuals might pass this DNA product to the next generation. Although random in pattern, studies showed that 1 infant in every 80,000 births can have this syndrome--a highly rare occurrence (â€Å"William Syndrome,† 2011). Like most genetic disorders, people with such condition can easily be distinguished due to their common appearance, where their faces may have an elfin quality, with prominent forehead and eyes, ample cheeks, expansi ve mouth, small nose, and broad earlobes (Semel & Rosner, 2003). In line with this, overall presentation of the condition can be divided into four sections: â€Å"cognitive development, language, auditory function, and visuospatial function† (Khan, Calureriu, Huang, & Robin, 2011). In context, cognition and language functions are quite delayed for their age, with highly sensitive hearing capabilities to auditory stimuli, and a disassociation between what is seen and its normative interpretations. As such, environmental adaptation of these groups is delayed, compared to their normal counterparts. Aside from these clinical symptoms, those with William Syndrome are also plagued with a number of medical disorders, which may range from clinically serious cardiac