Angelman Syndrome, formerly known as Happy putz Syndrome, is a genetic dis secernate affecting the mind and nerve system caused by the forming of the parents chromosomes through the first steps of a babys development. It is an example of genomic imprinting and normally is caused by deletion or inactivation of the mothers ordinal chromosome. Its founder, Dr. Harry Angelman, a British pediatrician in 1965, gave the disease its name, hence the reference of the victims of this disease as angels and for their happy appearance.
Angelman Syndrome in general affects the nervous system and mind. Many adults that are affected by this disease are described as coarse in facial appearance. This is a result of the loss of function of a gene called UBE3A.
The disease is apparent in a kidskin from around the ages of six to twelve months. Many symptoms of Angelman Syndrome are principally in the mind and nerve system: delay in physical development, intellectual disability and severe speech impairment, and bowel movement and balance issues (known as ataxia). Part of the delays of development is microcephaly, having a trivial head size. Recurrent seizures, or epilepsy, are as well a very frequent characteristic. Random laughter and joyfulness is also a symptom that progresses 100% of the time.
As of now, there is no cure to eliminate Angelman disease, but often, therapy is necessary. Seizures can be inured with medical therapy...If you want to get a full essay, order it on our website: Ordercustompaper.com
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