Your assignment is to prepare and submit a paper on williams syndrome. Williams Syndrome - Genetic Pediatric IllnessWilliams Syndrome is a genetic pediatric illness that was first observed in New Zea

Your assignment is to prepare and submit a paper on williams syndrome. Williams Syndrome - Genetic Pediatric Illness

Williams Syndrome is a genetic pediatric illness that was first observed in New Zealand by the reclusive Dr. J.C.P. Williams while working as a Registrar at Auckland's Greenlane Hospital in 1961. According to Physiopedia (2011), Dr. Williams noted that 4 of his patients had. “an association between supra valvular aortic stenosis and the common physical and mental characteristics of this patient population ... it “may constitute a previously unrecognized syndrome”. After some time, A.J. Beuren came across his own set of 11 patients who also had the same symptoms as described by Dr. Williams in the past. Thanks to his contribution to the study of what was then an unknown illness, the disease was named after the two men who contributed the most its understanding, Williams-Beuren Syndrome. However, the illness has also come to be known by other illnesses over the years. Physiopedia (2011) lists the other names as follows:

Williams-Beuren Syndrome

Beuren Syndrome

Elfin Facies Syndrome

Elfin Facies with hypercalcemia

Hypercalcemia-Supravalvar Aortic Stenosis

Infantile hypercalcemia

Supravalvar aortic stenosis syndrome

WBS

WMS

WS

Dr. Aneal Khan M.D., who authored an article regarding Williams Syndrome for Medscape Reference (2011) described the clinical manifestation of the illness to include. “a distinct facial appearance, cardiovascular anomalies that may be present at birth or may develop later in life, idiopathic hypercalcemia, and a characteristic neurodevelopmental and behavioral profile”. The disease does not seem to afflict any one specific gender, ethnicity, race, or socioeconomic background. However, it does seem to be most prevalent among children, affecting 7500 of every 20000 births. The most common symptoms of the birth defect according to Dr. Rob Hicks (2011) include but are not limited to:

Upturned nose

Widely spaced eyes

Wide mouth with full lips

Small chin

Slightly puffy cheeks

Irregular, widely spaced teeth

Various in depth studies of the illness link Williams Syndrome to the genetic make up of an individual. Dr. Rob Hicks (2011) , author of “Williams Syndrome” for BBC Health explained that WS afflicted individuals most often have a defect in the DNA chain of chromosome 7 with about 26 genes deleted from its long arm. Unfortunately, chromosome 7 is one of the most important elements of the human gene as this particular gene is tasked with the manufacture of the protein elastin which according to Dr. Hicks (2011), is “is responsible for providing strength and elasticity to blood vessel walls. “

Babies born with Williams Syndrome are often underweight upon birth with difficulty in gaining weight and have certain development defects such as speech problems with the ability to speak not becoming present until the age of 3. However, the most concerning matter of this illness is the widespread Cardiovascular complicationsassociated with it. The lack of development of elastin in Chromosome 7 prevents the manufacture and development and elastin within the child, weakening the cardiovascular walls of the child and presenting him with various cardiovascular illnesses over time. (Williams Syndrome Association, 2011). A WS afflicted child faces major health struggles, with the cardiovascular illnesses proving to be life-threatening.