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Détail de l'auteur
Auteur E. LEE |
Documents disponibles écrits par cet auteur (1)
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Prader-Willi syndrome and autism spectrum disorders: an evolving story / E. M. DYKENS in Journal of Neurodevelopmental Disorders, 3-3 (September 2011)
[article]
Titre : Prader-Willi syndrome and autism spectrum disorders: an evolving story Type de document : Texte imprimé et/ou numérique Auteurs : E. M. DYKENS, Auteur ; E. LEE, Auteur ; E. ROOF, Auteur Article en page(s) : p.225-37 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Prader-Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11-q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums, irritability, hyperphagia, and increased risks of obesity. Many individuals also have co-occurring autism spectrum disorders (ASDs), psychosis, and mood disorders. Although the PWS 15q11-q13 region confers risks for autism, relatively few studies have assessed autism symptoms in PWS or directly compared social, behavioral, and cognitive functioning across groups with autism or PWS. This article identifies areas of phenotypic overlap and difference between PWS and ASD in core autism symptoms and in such comorbidities as psychiatric disorders, and dysregulated sleep and eating. Though future studies are needed, PWS provides a promising alternative lens into specific symptoms and comorbidities of autism. En ligne : http://dx.doi.org/10.1007/s11689-011-9092-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=343
in Journal of Neurodevelopmental Disorders > 3-3 (September 2011) . - p.225-37[article] Prader-Willi syndrome and autism spectrum disorders: an evolving story [Texte imprimé et/ou numérique] / E. M. DYKENS, Auteur ; E. LEE, Auteur ; E. ROOF, Auteur . - p.225-37.
Langues : Anglais (eng)
in Journal of Neurodevelopmental Disorders > 3-3 (September 2011) . - p.225-37
Index. décimale : PER Périodiques Résumé : Prader-Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11-q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums, irritability, hyperphagia, and increased risks of obesity. Many individuals also have co-occurring autism spectrum disorders (ASDs), psychosis, and mood disorders. Although the PWS 15q11-q13 region confers risks for autism, relatively few studies have assessed autism symptoms in PWS or directly compared social, behavioral, and cognitive functioning across groups with autism or PWS. This article identifies areas of phenotypic overlap and difference between PWS and ASD in core autism symptoms and in such comorbidities as psychiatric disorders, and dysregulated sleep and eating. Though future studies are needed, PWS provides a promising alternative lens into specific symptoms and comorbidities of autism. En ligne : http://dx.doi.org/10.1007/s11689-011-9092-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=343