Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and
failure to thrive; hypogonadism causing genital hypoplasia and pubertal insufficiency; …

Prader-Willi syndrome is a complex disorder affecting multiple systems with many
manifestations relating to hypothalamic insufficiency. Major findings include infantile …

Prader–Willi syndrome (PWS) is a highly variable genetic disorder affecting multiple body
systems whose most consistent major manifestations include hypotonia with poor suck and …

Objective: The objective of the study was to provide recommendations for the diagnosis and
management of Prader-Willi syndrome throughout the life span to guide clinical practice …

Background Self‐injurious and aggressive behaviours are reported as components of some
behavioural phenotypes but there are few studies comparing across syndrome groups. In …

Recent advances are reviewed in understanding the heightened prevalence of
psychopathology and maladaptive behavior among children with intellectual disability …

Prader-Willi syndrome (PWS) is characterized by severe hypotonia and feeding difficulties in
early infancy, followed in later infancy or early childhood by excessive eating and gradual …

Autism is a heterogeneous disorder that can reveal a specific genetic disease. This paper
describes several genetic diseases consistently associated with autism (fragile X, tuberous …

Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with
a characteristic behavioral phenotype that includes severe hyperphagia and a variety of …

Objective. To determine whether phenotypic differences exist among individuals with Prader-
Willi syndrome with either type I or type II deletions of chromosome 15 or maternal disomy …