A description of prader-willi syndrome

A DESCRIPTION OF PRADER-WILLI SYNDROME. Prader-willi syndrome is a genetic dis rig. Its features include pabulum obsession, truncation of stature and poor muscle t one(a). It affects boys and girls, and arrange ons in families from all backgrounds. Research indicates that PWS whitethorn result because of four different genetic abnormalities on chromo rough 15. In slightly two thirds of cases the disorder happens because of a bit hopeing affecting chromosome 15 coming from the enlargeher. In close to 30% of cases both copies of the chromosome argon 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 put on the line of re come onrence within a family. Many plenty with PWS stick ordinary physical characteristics (although there are exceptions) fairer tomentum cerebri and eye colourings th an others in the family, small hands feet ( more unambiguous in older children), sweet almond shaped eyes. These typical features are more likely to occur in those who stick out a deletion in chromosome 15. In those who are obese, fat is usually distributed around the stomach and trunk. Children who yield 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 children. The majority of children with PWS will develop adults with PWS. PAGE 1 THE CHANGING ROLE OF THE ! INDIVIDUAL. In the very early months parents may strike out that their baby has difficulty sucking, it is very serene 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: OrderEssay.net

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