Williams syndrome is a genetic disorder that is caused by the absence of signifi batcht on the seventh pair of chromosomes (H tout ensembleahan and Kauffman, 130). It is present at birth, and affects males and females equally. It can occur in all ethnic groups and has been identified in countries throughout the world (WSA).
Children with Williams Syndrome atomic number 18 said to have very(prenominal) similar facial features. Wide mouth, wide-cut lips, small turned nose, small chin and puffiness around their eyes be the most common features. The facial features become more self-aggrandizing over age (Hallahan and Kauffman, 130).
The majority of individuals with Williams syndrome have some typesetters case of heart or blood vessel problem. There is constrictive in the aorta, or narrowing in the pulmonary arteries. The story of narrowing differs from trivial to severe. Risk of high blood wardrobe is increased meaning, over time monitoring cardiac perspective is necessary. (WSA) Symptoms of Williams syndrome include low birth weight, sensitive hearing, and dental abnormalities. approximately of the time weight increases slowly after birth collectable to a high gag reflex. There is nothing that causes the syndrome. Parents cannot preclude it nor cause it.
Diagnosing Williams Syndrome is not difficult. It can be support by a blood test given by a doctor. There is also a tool called FISH, which specializes in analyzing chromosomes.
FISH is not readily available by all hospitals, blood tests can be sent to hospitals that have this tool.(WSA) The record of a child with Williams Syndrome tends to be very friendly. Children with this disability are rarely shy and timid and are more seeming to get along with an adult rather than their peers. Although, children with this disability normally have developmental delays such as walking, talking and prat training they show great strengths in speech and actors line later in their...
If you want to get a full essay, wisit our page: write my paper
No comments:
Post a Comment