Neurobehavioral Phenotype in Prader-Willi Syndrome

被引:40
|
作者
Whittington, Joyce [1 ]
Holland, Anthony [2 ]
机构
[1] Univ Cambridge, Dept Psychiat, Cambridge CB2 8AH, England
[2] Univ Cambridge, Cambridge Intellectual & Dev Disabil Res Grp, Acad Dept Psychiat, Cambridge CB2 8AH, England
基金
英国惠康基金;
关键词
Prader-Willi syndrome; behavioral phenotypes; genomic imprinting; abnormal satiety; psychotic illness; BODY-MASS INDEX; COMPULSIVE BEHAVIOR; PSYCHIATRIC-ILLNESS; GHRELIN LEVELS; PEOPLE; CHILDREN; PREVALENCE; DELETION; GENE; DISORDERS;
D O I
10.1002/ajmg.c.30283
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The focus of this article is on the lifetime development of people with Prader-Willi syndrome (PWS) and specifically on the neurobehavioral phenotype. We consider studies of this aspect of the phenotype (the "behavioral phenotype'' of the syndrome) that have confirmed that there are specific behaviors and psychiatric disorders, the propensities to which are increased in those with PWS, and cannot be accounted for by other variables such as IQ or adaptive behavior. Beginning with a description of what is observed in people with PWS, we review the evolving PWS phenotype and consider how some aspects of the phenotype might be best explained, and how this complex phenotype may relate to the equally complex genotype. We then consider in more detail some of the neurobehavioral aspects of the phenotype listed above that raise the greatest management problems for parents and carers. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:438 / 447
页数:10
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