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Prader-Willi Syndrome: Unraveling the Complexity of a Rare Genetic Disorder
Prader-Willi Syndrome (PWS) is a complex, rare genetic condition characterized by endocrine dysfunction, hypotonia, hyperphagia, and developmental delays. Emerging precision care strategies, including hormone therapy, nutritional management, and behavioral interventions, are reshaping outcomes for affected individuals. As science progresses, early diagnosis and multidisciplinary management...
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