Prader-Willi syndrome

被引：16
|
作者：
Couper, RTL [1 ]
机构：
[1] Univ Adelaide, Womens & Childrens Hosp, Dept Paediat, N Adelaide, SA 5006, Australia
来源：
JOURNAL OF PAEDIATRICS AND CHILD HEALTH | 1999年 / 35卷 / 04期
关键词：
behavioural problems; genetics; Prader-Willi syndrome;
D O I：
10.1046/j.1440-1754.1999.00397.x
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardation. It occurs sporadically, either as a result of microdeletion of chromosome 15p (70%) or as a result of maternal disomy of chromosome 15 (30%). The major problems encountered by parents are those of hyperphagia, food-seeking and obesity, and conduct disorder, particularly tantrums or oppositional behaviour.
引用
收藏
页码：331 / 334
页数：4
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