Prader–Willi syndrome (PWS) is a rare genetic disorder that results from lack of expression
of paternally‐derived genes on chromosome 15q11‐13; caused by a deletion (DEL) …

Obesity is the most common cause of metabolic complications and poor quality of life in
Prader–Willi syndrome (PWS). Hyperphagia and obesity develop after an initial phase of …

Background Epilepsy and autism spectrum disorder (ASD) are the common neurological
manifestations of tuberous sclerosis complex (TSC). EXIST-3 study has recently …

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

We present a review of psychiatric associations with comorbid mental and behavioural
disorders affecting people with Prader-Willi syndrome (PWS). This literature review suggests …

Prader–Willi syndrome is a genetic disorder caused by chromosomal changes in segment
15q11-q13 including cognitive, mental, and behavioral symptoms, as well as a specific …

Abstract Prader–Willi syndrome (PWS, OMIM# 176270) and Down syndrome (DS, OMIM#
190685) are neurodevelopmental genetic disorders with higher rates of autism spectrum …

Although various studies have investigated symptoms of autism spectrum disorder (ASD) in
Prader–Willi syndrome (PWS), little is known about the consequences of these symptoms …

Prader-Willi syndrome (PWS), a rare genetic disorder caused by the lack of expression of
paternal genes from chromosome 15q11-13, has been investigated for autism spectrum …

El síndrome de Prader-Willi es un trastorno genético causado por alteraciones
cromosómicas en el segmento 15q11-q13 que incluye sintomatología cognitiva, mental y …