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040-68334455Frequently Asked Questions
Prader Willi Syndrome is a rare genetic condition that affects growth, metabolism and hormone regulation, resulting in distinct physical and developmental characteristics.
Prader Willi Syndrome is uncommon, affecting approximately 1 in 10,000 to 30,000 people worldwide.
Prader Willi Syndrome occurs due to genetic changes and can affect both males and females, with no preference for specific ethnic or geographic groups.
Yes, individuals with Prader Willi Syndrome may require specialised support in areas like nutrition, physical activity and growth management to optimise daily functioning.
Prader Willi Syndrome results from genetic alterations but most cases occur sporadically rather than being directly inherited from a parent.
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