Psychiatric Features in Children with Genetic Syndromes: Toward Functional Phenotypes

被引:14
|
作者
Siegel, Matthew S. [1 ,2 ,3 ]
Smith, Wendy E. [4 ,5 ]
机构
[1] Maine Med Ctr, Div Child Psychiat, Dept Psychiat, Portland, ME 04092 USA
[2] Tufts Univ, Sch Med, Dept Psychiat, Boston, MA 02110 USA
[3] Spring Harbor Hosp, Dev Disorders Program, Westbrook, ME 04092 USA
[4] Barbara Bush Childrens Hosp, Maine Med Ctr, Dept Pediat, Div Genet, Portland, ME 04102 USA
[5] Maine Med Partners, Pediat Specialty Care, Portland, ME 04102 USA
关键词
Children; Phenotype; Behavioral; Genetic; Neuropsychiatric; PRADER-WILLI-SYNDROME; SMITH-MAGENIS-SYNDROME; FRAGILE-X-SYNDROME; CARDIO-FACIAL SYNDROME; SELF-INJURIOUS-BEHAVIOR; TURNER-SYNDROME; RETT-SYNDROME; MENTAL-RETARDATION; 22Q11.2; DELETION; DOWN-SYNDROME;
D O I
10.1016/j.chc.2010.02.001
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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.
引用
收藏
页码:229 / +
页数:34
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