Prader-Willi syndrome is a rare genetic disease that manifests itself mainly by two very specific symptoms: a large muscle weakness and hyperphagia, an uncontrollable urge to eat, patients do not control their diet, which often leads to obesity. Unfortunately this syndrome is more complex than just overeating. Prader-Willi syndrome is a rare genetic disease so little known, which affects one birth in 25 000.
In fact, everything is related to an anomaly of chromosome 15, an abnormality that is not inherited and results in many chain reactions. First it disrupts the hypothalamus. This region at the base of the brain can control the main functions of the body: hunger, thirst, wakefulness, regulating temperature. This gland regulates the activity of another gland, the pituitary gland, located just below it. The consequences are varied and they change with age.
Basically, just after birth, there is hypotonia, a lack of muscle tone, some infants are too weak to suckle. This will persist and delayed motor development of the child and therefore affects the ability of walking.
Then the binge starts, the feeling of hunger pushes the child in a perpetual search of food. The baby consumes far more calories than other children, which causes it to become overweight. Obesity may then proceed with more serious consequences: diabetes, loss of mobility, breathing problems, heart failure. In adolescence, there is also learning difficulties and behavioral problems which vary depending on the subject. Nutrisystem can help by arranging the best types of meals to curb the onset of uncontrollable urges to eat both in babies and adolescents. You can find the latest Nutrisystem coupon code on my homepage.
A multidisciplinary approach
The symptoms of Prader-Willi syndrome does not always manifest and according to statistics and they show variable degrees of severity. In all cases, it is essential that patients have a multidisciplinary approach to managing the disease: physical therapy, speech therapy are among the priorities and of course, their food should be monitored by a nutritionist. And this last part is where Nutrisystem can vastly help.
The importance of early diagnosis
Myriam is 26 years old. Although she was diagnosed late, at the age of 9, and with the help of her parents and doctors, she quickly benefited from good care. Today, she is doing well. Myriam was able to find a job despite Prader-Willi syndrome. She found a job in an Establishment and Service Support through Work (ESAT), which does not welcome “the Prader-Willi” usually but in this case, agreed to make an exception.
Obviously the earlier the diagnostic is made, the more the prognosis for patients is improving and they are progressing. Fortunately, this disease is now better known and doctors can now diagnose the disease in the first months after birth. They can benefit from a treatment growth hormone which helps them grow better, to be thinner and increase muscle tone. Nutrisystem can help create a diet plan which will ensure good growth and development, especially in babies.