Psychiatric features in children with genetic syndromes: toward functional phenotypes

Child Adolesc Psychiatr Clin N Am. 2010 Apr;19(2):229-61, viii. doi: 10.1016/j.chc.2010.02.001.

Abstract

Neurodevelopmental disorders with identified genetic etiologies present a unique opportunity to study gene-brain-behavior connections in child psychiatry. Parsing complex human behavior into dissociable components is facilitated by examining a relatively homogenous genetic population. As children with developmental delay carry a greater burden of mental illness than the general population, familiarity with the most common genetic disorders will serve practitioners seeing a general child population. In this article basic genetic testing and 11 of the most common genetic disorders are reviewed, including the evidence base for treatment. Based on their training in child development, family systems, and multimodal treatment, child psychiatrists are well positioned to integrate cognitive, behavioral, social, psychiatric, and physical phenotypes, with a focus on functional impairment.

Publication types

  • Review

MeSH terms

  • Angelman Syndrome / epidemiology
  • Angelman Syndrome / genetics
  • Attention Deficit Disorder with Hyperactivity / epidemiology
  • Child
  • Cognition Disorders / epidemiology
  • Down Syndrome / genetics*
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Syndrome / epidemiology
  • Fragile X Syndrome / genetics
  • Health Status
  • Humans
  • Mental Disorders / epidemiology
  • Mental Disorders / genetics*
  • Methyl-CpG-Binding Protein 2 / genetics
  • Phenotype*
  • Point Mutation / genetics
  • Polymerase Chain Reaction
  • Prader-Willi Syndrome / epidemiology
  • Prader-Willi Syndrome / genetics
  • Rett Syndrome / epidemiology
  • Rett Syndrome / genetics*
  • Williams Syndrome / epidemiology
  • Williams Syndrome / genetics

Substances

  • FMR1 protein, human
  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2
  • Fragile X Mental Retardation Protein