Williams Syndrome Summary of Important Information I chose to do Williams Syndrome because it is a impairment that is unfamiliar to me and I wanted the opportunity to witness more than about it. I have taken my nurture from the earnings and cited my sources. Williams Syndrome is a rare brokertic disorder which leads to organic evolutional problems, such as: a childs growth, physical carriage and cognitive cultivation. This syndrome is caused by missing factors. One of the missing genes is the gene that produces elastin. In this condition blood vessels narrow due to the spark of elastin in the vessels. When blood vessels are formed, elastin protein is made during the embryonic development and childhood. Because elastin is lacking individuals with Williams Syndrome tend to have heart defects and circulatory organization problems. The incidence rate for Williams Syndrome is extremely low and affects about 1 in 8,000 children. Odds are that parents may not discern of any family history of this disease. (Genetics Learning Center, 1969) (A.D.A.M, 2001) The symptoms of Williams Syndrome are usually range as a child grows from infancy.

Some symptoms of Williams Syndrome are amicable retardation, heart defect and unusual facial features such as: a runty upturned nose, wide mouth, full lips, wee chin and widely spaced teeth. They excessively show signs of developmental delay and delayed speech, that may later turn into knockout speaking abilities and strong learning, by having heard what they need to. Furthermore, the following could overly occu r: kidney abnormalities, eating problems, fa! ilure to gain allow weight and low muscle tone. Individuals that carry these symptoms will also be very outgoing and may show signs of delicacy deficit disorder (ADD). These are only a less of the symptoms that children born with this disability experience. (Genetics Learning Center, 1969) Physicians are able to observe Williams Syndrome due to is physical characteristics, but there are...If you want to cross a full essay, order it on our website:
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