【摘 要】
：
Prader-willi综合征是由于人类父源15号染色体q11-13区域异常所导致的一个复杂的多系统异常疾病[1].主要临床特征包括新生儿期的肌张力低、吸收能力差、发育迟缓、身材矮小、
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Prader-willi综合征是由于人类父源15号染色体q11-13区域异常所导致的一个复杂的多系统异常疾病[1].主要临床特征包括新生儿期的肌张力低、吸收能力差、发育迟缓、身材矮小、行为异常,童年时期开始肥胖,下丘脑性腺机能减退,典型的行为障碍及特征性外貌.Prader-willi患儿存在多方面的问题,需针对不同个体制定出一系列的治疗方案,以求最佳效果[2].尤以摄食过度、肥胖更为突出,因此早期诊断和合理的饮食控制是关键.
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