Systematic review and meta-analysis / Emma J. Glasson en Journal of the American Academy of Child & Adolescent Psychiatry, Año 2020 - Vol. 59 - No. 9 (Septiembre)

Público ISBD [artículo]  inJournal of the American Academy of Child & Adolescent Psychiatry > Año 2020 - Vol. 59 - No. 9 (Septiembre) . - pp.1036-1048 Título : Systematic review and meta-analysis : mental health in children with neurogenetic disorders associated with intellectual disability Tipo de documento: texto impreso Autores: Emma J. Glasson, Autor ; Nicholas Buckley, Autor ; Wai Chen, Autor Fecha de publicación: 2020 Artículo en la página: pp.1036-1048 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Trastorno genético, Discapacidad intelectual, Salud mental, Predominio Resumen: The behavioral phenotype of neurogenetic disorders associated with intellectual disability often includes psychiatric comorbidity. The objectives of this systematic review and meta-analysis were to systematically review the prevalence of psychiatric disorders and symptoms in children and adolescents with these disorders and compare phenotypic signatures between syndromes. Link: ./index.php?lvl=notice_display&id=25565 [artículo] Systematic review and meta-analysis : mental health in children with neurogenetic disorders associated with intellectual disability [texto impreso] / Emma J. Glasson, Autor ; Nicholas Buckley, Autor ; Wai Chen, Autor . - 2020 . - pp.1036-1048. Idioma : Inglés (eng) Idioma original : Inglés (eng) in Journal of the American Academy of Child & Adolescent Psychiatry > Año 2020 - Vol. 59 - No. 9 (Septiembre) . - pp.1036-1048 Palabras clave: Trastorno genético, Discapacidad intelectual, Salud mental, Predominio Resumen: The behavioral phenotype of neurogenetic disorders associated with intellectual disability often includes psychiatric comorbidity. The objectives of this systematic review and meta-analysis were to systematically review the prevalence of psychiatric disorders and symptoms in children and adolescents with these disorders and compare phenotypic signatures between syndromes. Link: ./index.php?lvl=notice_display&id=25565

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