Our June Societe Gives Back Charity Partner is The Foundation for Prader-Willi Research.
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 and ethnicities. PWS is recognized as the most common genetic cause of life-threatening childhood obesity.
PWS was first described by Swiss doctors Andrea Prader, Alexis Labhart, and Heinrich Willi in 1956 based on the clinical characteristics of nine children they examined. The common characteristics defined in the initial report included small hands and feet, abnormal growth and body composition (small stature, very low lean body mass, and early-onset childhood obesity), hypotonia (weak muscles) at birth, insatiable hunger, extreme obesity, and intellectual disability.
PWS results from an abnormality of chromosome 15, and definitive diagnosis is now based on genetic testing.
Come out each Tuesday in June to help support this cause and learn more about how you can help!
A portion of each Tuesday's Sales in June will be donated to this great cause and their efforts!