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Brian Mengel,
Civil Servant
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The Diagnosis of Prader-Willi Syndrome should be made through a qualified medical professional.
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Albert Graham,
Backyard Pool Drainer
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Prader-Willi syndrome is the most common genetic cause of obesity that has been identified.
Prader-Willi Syndrome is a genetic disorder and affects the individual in very many ways.
Prader-Willi Syndrome (PWS) is a chromosomal disorder, which can affect people of both sexes and of any race or country.
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Keith Tennant,
Factory Worker
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What are the symptoms of Prader- Willi Syndrome?
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Adam Findley,
Professional Motivator
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PRADER-WILLI SYNDROME: An inherited condition typified by hypotonia with failure to thrive.
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Sasha Prevette,
Kindergarten student
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Prader-Willi Syndrome (PWS) affects one in every 16,000 people that are born.
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Arthur Dawkins,
Astro-physicist
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The Prader-Willi Syndrome Association (USA) invites scientific presentations of current research on topics relating to the syndrome.
A cause of Prader-Willi Syndrome in some people with the syndrome appears to be a deletion in chromosome 15.
Prader-Willi Syndrome was identified in 1954 and to date, not enough has been done to promote research specific to find a cure for PWS.
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David Rosenberg,
Dermatologist
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I was the first person born with Prader-Willi Syndrome to have obtained all three official certificates.
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