(1) Background: children with Prader-Willi syndrome (PWS) have high obesity rates due to hyperphagia and decreased metabolic rates. Although anti-obesity medications (AOMs) are prescribed to this population, there are no consensus guidelines on acceptability, safety, and efficacy. We present literature review and case series on AOMs in youth with PWS. (2) Methods: we performed PubMed review from January 2000 to April 2021 utilizing keywords: “Prader-Willi syndrome” or “PWS” and “medication” including: topiramate, metformin, phentermine, liraglutide, orlistat, oxytocin, semaglutide, naltrexone-bupropion. For our case series, patients were identified through retrospective chart reviews from a multi-disciplinary PWS clinic. Eligibility criteri...
Hyperphagia is a frequent symptom in patients with Prader-Willi Syndrome (PWS) and results in marked...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
In early childhood, individuals with Prader-Willi syndrome (PWS) experience excess weight gain and s...
Prader–Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologi...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Introduction: Prader-Willi syndrome (PWS) is the most well-known condition of genetic obesity. Over ...
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia...
We read with interest the case report by Puri et al. (2016) describing a 13-year-old girl with Prade...
Objectives Prader-Willi Syndrome (PWS) is characterised by hyperphagia often leading to obesity; a k...
BACKGROUND AND AIMS: Prader-Willi syndrome (PWS), the most frequent syndromic obesity, is associated...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi syndrome (PWS) is the most common cause of morbid obesity in childhood. It is the conse...
ABSTRACT Objective: To carry out a review about Prader-Willi Syndrome based on the most recent dat...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Hyperphagia is a frequent symptom in patients with Prader-Willi Syndrome (PWS) and results in marked...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
In early childhood, individuals with Prader-Willi syndrome (PWS) experience excess weight gain and s...
Prader–Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologi...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Introduction: Prader-Willi syndrome (PWS) is the most well-known condition of genetic obesity. Over ...
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia...
We read with interest the case report by Puri et al. (2016) describing a 13-year-old girl with Prade...
Objectives Prader-Willi Syndrome (PWS) is characterised by hyperphagia often leading to obesity; a k...
BACKGROUND AND AIMS: Prader-Willi syndrome (PWS), the most frequent syndromic obesity, is associated...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi syndrome (PWS) is the most common cause of morbid obesity in childhood. It is the conse...
ABSTRACT Objective: To carry out a review about Prader-Willi Syndrome based on the most recent dat...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Hyperphagia is a frequent symptom in patients with Prader-Willi Syndrome (PWS) and results in marked...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...