PRADER WILLI SYNDROME(PWDS), Causes, Signs and Symptoms, Diagnosis and Treatment.
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YouTubeMedical Centric Podcast
PRADER WILLI SYNDROME(PWDS), Causes, Signs and Symptoms, Diagnosis and Treatment.
. Chapters 0:00 Introduction 1:09 Causes of Prader–Willi syndrome 2:05 Symptoms of Prader–Willi syndrome 3:00 Diagnosis of Prader–Willi syndrome 3:50 Treatment of Prader–Willi syndrome Prader–Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes.In newborns, symptoms include weak muscles, poor feeding ...
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Welcome to our page! We share a real, behind-the-scenes look at life with Prader-Willi Syndrome (PWS) — the highs, the challenges, and all the moments in between. 💛 What is PWS? Prader-Willi Syndrome is a rare genetic condition that affects appetite, growth, behavior, and learning. Individuals with PWS may feel hungry more often, need extra support with routines and emotions, and benefit from a structured, safe environment. But they are also strong, loving, funny, and full of personality — just
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