Hypothalamic syndrome (HS) is a rare disorder caused by disease-related and/or treatment-
related injury to the hypothalamus, most commonly associated with rare, non-cancerous …

Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …

In early childhood, individuals with Prader‐Willi syndrome (PWS) experience excess weight
gain and severe hyperphagia with food compulsivity, which often leads to early onset morbid …

Background The global pandemic and subsequent denials, delays, and disruptions in
essential daily activities created significant challenges for children with neurodevelopmental …

The aim of this meta-analysis was to investigate factors associated with resilience in familial
caregivers of children with developmental disabilities. The protocol was registered in the …

Abstract Context Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by
endocrine and neuropsychiatric problems including hyperphagia, anxiousness, and …

Introduction Individuals with proopiomelanocortin (POMC) or leptin receptor (LEPR)
deficiency are young and experience severe obesity, hyperphagia, and comorbidities, which …

Abstract Background Prader–Willi syndrome (PWS) is a neurogenetic syndrome with an
associated behavioural phenotype and a high incidence of behaviours of concern and …

Objectives Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by
maladaptive behaviors, amongst which hyperphagia is a life-long concern for individuals …

Prader–Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involving the
hypothalamus. It is caused by loss of expression of paternally inherited genes in …