When it comes down to diagnosing someone with this disorder, there aren’t always a specific set of rules to follow. This is due to not everyone one having the exact same symptoms. Typically it is easy to diagnose someone at birth by their looks alone, but some aren’t diagnosed until later on in life. One of the first physical signs noticed at birth is hypotonia. Hypotonia is when a person has low muscle tone and can make their body appear floppy (Cassidy and Driscoll, 2009; Kundert, 2008). As an individual with PWS begins to grow, their facial features and growth rate become noticeable. A child with PWS typically has a small stature and small hands and feet. The facial features of a PWS individual are very distinct. The individual will have a wide set face and nasal bridge, almond shaped eyes, and a small mouth (Kundert, 2008). Mainly the features of a PWS individual appear disproportional.
On the contrary to popular belief, PWS involves more than just physical signs. At a young age, symptoms of mental and behavioral problems emerge. Typically, individua...
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...rol and prevention of getting diabetes (Kundert, 2008). If a care giver is having problems dealing coping with PWS they shouldn’t be afraid to ask for help.
In this paper is a detailed description of what Prader- Willi Syndrome really is. Noted above is all the signs and symptoms that explain what having PWS really means. Along with the signs and symptoms is described the family and the individual’s quality of life and how to cope when caring for a person with PWS. Though a lot of progress has been made in the discovery about the cause and how to deal with PWS, there is still a long way to go when it comes to learning all there is to know. It is stated by Cassidy and Driscoll (2009) that there is still a lot to discover in the cause of PWS, but when that knowledge is known it could help unravel a true treatment in how to prevent or turn back the clock on PWS forever.
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