Prader-Willi syndrome: A syndromic cause of morbid obesity

被引：0

作者：

Rawat, Ankur ^{[1
]}

Shaw, Subhash Chandra ^{[1
]}

Kalra, Suprita ^{[2
]}

Gupta, Rakesh ^{[1
]}

机构：

[1] Armed Forces Med Coll, Dept Pediat, Pune 411040, Maharashtra, India

[2] Command Hosp, Dept Pediat, Pune, Maharashtra, India

来源：

JOURNAL OF MARINE MEDICAL SOCIETY | 2018年 / 20卷 / 01期

关键词：

Hypogonadism; hypotonia; obesity; Prader-Willi syndrome;

D O I：

10.4103/jmms.jmms_69_17

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder with a prevalence of about 1/10,000-1/30,000. It is also the first known disorder of human genomic imprinting. We report a case of a child with PWS presenting with hypotonia and feeding difficulty in the neonatal period and infancy with characteristic facial features, hyperphagia, early onset of morbid obesity, short hands and feet, intellectual disability, and other behavioral problems.

引用

页码：76 / 78

页数：3

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