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Abstract Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass, muscular hypotonia, mental retardation, behavioral abnormalities, dysmorphic features, and excessive appetite with progressive obesity

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& Seidman, H

Dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 receptor agonists, like once-weekly tirzepatide resulted in the mean body weight changes of -17.5%

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NAFLD and liver transplantation: Current burden and expected challenges