Genetics of obesity and overgrowth syndromes

被引:31
|
作者
Sabin, Matthew A. [1 ,2 ]
Werther, George A. [1 ,2 ]
Kiess, Wieland [3 ]
机构
[1] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] Univ Leipzig, Univ Hosp, Dept Women & Child Hlth, Hosp Children & Adolescents, Leipzig, Germany
关键词
Obesity; Overgrowth; Genetic; Syndromes; Stature; CONGENITAL LEPTIN DEFICIENCY; IN-VITRO FERTILIZATION; EARLY-ONSET OBESITY; NEUROFIBROMATOSIS TYPE-1; SOTOS-SYNDROME; KLINEFELTER-SYNDROME; MARFAN-SYNDROME; NSD1; MUTATIONS; RECEPTOR GENE; GROWTH;
D O I
10.1016/j.beem.2010.09.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Childhood overweight and obesity is highly prevalent within society. In the majority of individuals, weight gain is the result of exposure to an 'obesogenic' environment, superimposed on a background of genetic susceptibility brought about by evolutionary adaptation. These individuals tend to be tall in childhood with a normal final adult height, as opposed to those who have an underlying monogenic cause where short stature is more common (although not universal). Identifying genetic causes of weight gain, or tall stature and overgrowth, within this setting can be extremely problematic and yet it is imperative that clinicians remain alert, as identification of a genetic diagnosis has major implications for the individual, family and potential offspring. Alongside this, the recognition of new genetic mutations in this area is furthering our knowledge on the important mechanisms that regulate childhood growth and body composition. This review describes the genetic syndromes associated with obesity and overgrowth. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:207 / 220
页数:14
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