Prader willi syndrome prevention

If before we talk about what is alopecia? on occasion this time we will review some challenge Prader Willi syndrome. Prader Willi syndrome is a chronic genetic disorders are quite rare. The disease is rare because of Prader-Willi syndrome found only 1 in 10,000 and 1 in between 25,000 in each new birth.

The disease was first recognized in 1956 with symptoms that are quite varied. Some of the most common symptoms are muscle weakness and unsatisfiable appetite (food cravings), leading to obesity.

Other symptoms and characteristics, including behavioral problems, difficult to express something, this type of disorder OCD, a short statures, incomplete sexual development, and much more.

Doctor Alexis Labhart, Andrea Prader and Heinrich Willi is the first to recognize the Prader willi syndrome. Two of the last person whose name is used to identify this genetic syndrome. Although relatively rare disease but there is still much unknown by medical experts about this disease.

Here are some things that need attention and can be used as a reference for you when faced with this disease:

1. Consult with Child Psychiatrist.

Because Prader willi syndrome including rare disease and rarely detected, the patient or parent should patients consult with psychiatrist experts. Prepare what things to look for in the consultation and how to prepare for the consultation to get maximum results.

Included in it is that behavioral therapy should be closely supervised by experts.

2. Food Security.

Consider a healthy diet for children with Prader willi syndrome (strict diet). All you need do is to understand the basic principles that are helpful in maintaining good body weight and control the behavior of children with PWS.

How to control this food can be a lock on the pantry or refrigerator, which is meant to restrict access to get food.

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