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Destiny Davis
Prader-Willi (PRAH-dur VIL-e) syndrome is a rare genetic disorder that results in a number of physical, mental and behavioral problems. A key feature of Prader-Willi syndrome is a constant sense of hunger. A genetic disorder that causes obesity, intellectual disability, and shortness in height.
The list of symptoms are Food cravings and weight gain, underdeveloped sex organs, poor growth and physical development, impairment, and deylayed motor development.
The diagnosis is confirmed by a blood test. The preferred method of testing is a “methylation analysis,” which detects >99% of cases, including all of the major genetic subtypes.
They have some foudations set up for it; The Foundation for Prader-Willi Research, MedlinePlus: Prader-Willi Syndrome, and -Willi Syndrome Association (USA).
The assistive technology can help kids with a processing disorder better understand what they hear. As well as the tools which include listening devices, captions and text-to-speech apps. This baically can help amplify speech to make it clearer.
Prader-Willi syndrome (PWS) is a genetic disorder that occurs in approximately one out of every 15,000 births. PWS affects males and females with equal frequency and affects all races.
Treatments that can help ?
https://www.mayoclinic.org/diseases-conditions/prader-willi-syndrome/symptoms-causes/syc-20355997
https://gompers.org/understanding-assistive-technology-and-its-benefits-on-people-with-disabilities/