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 …

Genomic imprinting disorders are caused by the disruption of genomic imprinting processes
leading to a deficit or increase of an active allele. Their unique molecular mechanisms …

Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder. Global
hypothalamic dysfunction is a core feature of PWS and has been implicated as a driver of …

Abstract Objective Prader-Willi syndrome (PWS) is a rare genetic imprinting disorder
resulting from the expression loss of genes on the paternally inherited chromosome 15q11 …

The hypothalamus regulates fundamental aspects of physiological homeostasis and
behavior, including stress response, reproduction, growth, sleep, and feeding, several of …

The neuronal-specific SNORD115 has gathered interest because its deficiency may
contribute to the pathophysiology of Prader-Willi syndrome (PWS), possibly by altering post …

Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by the
deletion or inactivation of paternally expressed imprinted genes at the chromosomal region …

Prader-Willi syndrome (PWS) is the prototypic genomic disorder resulting from deficiency of
paternally expressed genes in the human chromosome 15q11-q13 region. The unique …

Prader-Willi syndrome (PWS) is a rare neurogenetic syndrome that results in significant
challenges in the school setting, often requiring a myriad of academic, social-emotional, and …

Recent studies demonstrate that paternal nutrition prior to conception may determine
offspring development and health through epigenetic modification. This study aims to …