Prader–Willi syndrome: A syndromic cause of morbid obesity
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 infanc...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2018-01-01
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| coleção: | Journal of Marine Medical Society |
| Assuntos: | |
| Acesso em linha: | http://www.marinemedicalsociety.in/article.asp?issn=0975-3605;year=2018;volume=20;issue=1;spage=76;epage=78;aulast=Rawat |
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