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CASE REPORT
Year : 2018  |  Volume : 20  |  Issue : 1  |  Page : 76-78

Prader–Willi syndrome: A syndromic cause of morbid obesity


1 Department of Pediatrics, Armed Forces Medical College, Pune, Maharashtra, India
2 Department of Pediatrics, Command Hospital, Pune, Maharashtra, India

Correspondence Address:
Lt Col Subhash Chandra Shaw
Department of Pediatrics, Armed Forces Medical College, Pune - 411 040, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jmms.jmms_69_17

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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.


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