The illness acquired its identify by three medical doctors who described the syndrome in 1956. (Prader, Labhart and Willi)
It is normally a genetic or congenital situation.
It is a genetic dysfunction attributable to the wrong division of the fifteenth chromosome when the child is fertilized within the womb.
It is a uncommon illness.
The illness happens in certainly one of 12 thousand to fifteen thousand instances.
WHAT ARE THE SYMPTOMS?
Issues on this illness first seem in infancy.
Whereas infants have problem in feeding, there is additionally weak point within the muscle groups.
Once more, as one of many consciousness that may be seen in infancy, they expertise a scarcity of genital organs.
The individual with this illness begins to lose the sensation of satiety as he will get older and eats lots.
One other indicative function is that folks with the illness have small palms and legs.
IS THERE A TREATMENT?
As a result of Prader-Willi syndrome is a genetic situation, a retrospective therapy is not attainable.
The therapies utilized are principally geared toward lowering the severity of the syndrome.
Remedy is additionally an efficient technique to right behavioral issues and cut back extra weight.
For the reason that signs and the diploma of the syndrome differ from individual to individual, a transparent therapy has not been revealed but.
#Prader #Willi #syndrome
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