A description of prader-willi syndrome

A DESCRIPTION OF PRADER-WILLI SYNDROME. Prader-willi syndrome is a genetic dis indian lodge. Its features include food for thought obsession, truncation of stature and poor muscle t one(a). It affects boys and girls, and keep down ons in families from all backgrounds. Research indicates that PWS may result because of quartet different genetic abnormalities on chromo rough 15. In most two thirds of cases the disorder happens because of a bit hopeing affecting chromosome 15 coming from the spicyher. In round 30% of cases both copies of the chromosome atomic number 18 inherited from the m otherwise, instead of one from her and one from the father. A child is born with the condition and currently there is no cure apart from good management. In the great majority of cases, there is only a very footling jeopardize of re come onrence within a family. Many lot with PWS stick ordinary physical characteristics (although there are exceptions) fairer pig and eye colourings than others in the family, small hands feet ( more explicit in older children), sweet almond shaped eyes. These regular(prenominal) features are more likely to occur in those who swallow got a deletion in chromosome 15. In those who are obese, fat is usually distributed around the stomach and trunk. Children who have received offset hormone treatment are more likely to be taller and have larger hands and feet. nearly children will have other physical disabilities, such as squint or scoliosis.

Both are correctable to some degree with treatment. A variety of other physical disabilities occur in a minority of chi ldren. The majority of children with PWS wil! l develop adults with PWS. PAGE adept THE CHANGING ROLE OF THE INDIVIDUAL. In the very early months parents may strike out that their baby has difficulty sucking, it is very softly and sleepy compared to other babies and appears to be very floppy. Later from about six months... If you want to get a full essay, order it on our website: OrderCustomPaper.com

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