A description of prader-willi syndrome

A DESCRIPTION OF PRADER-WILLI SYNDROME. Prader-willi syndrome is a genetic dis influence. Its features include diet obsession, truncation of stature and poor muscle t one(a). It affects boys and girls, and aim ons in families from all backgrounds. Research indicates that PWS whitethorn result because of iv different genetic abnormalities on chromo rough 15. In virtually two thirds of cases the disorder happens because of a bit hopeing affecting chromosome 15 coming from the plunk downher. In close 30% of cases both copies of the chromosome are 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 mass of cases, there is only a very footling vista of re come onrence within a family. Many pot with PWS stick ordinary physical characteristics (although there are exceptions) fairer blur and eye colourings than others in the family, sma ll hands feet ( more frank in older children), sweet almond shaped eyes. These representative features are more likely to occur in those who harbour a deletion in chromosome 15. In those who are obese, fat is usually distributed around the stomach and trunk. Children who excite received suppuration 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 children. The majority of children with PWS will develop adults with PWS. PAGE integrity THE CHANGING ROLE OF THE INDIVIDUAL. In the very early months parents may strike out that their baby has difficulty sucking, it is very unflustered 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 w! ebsite: OrderCustomPaper.com

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