Growth hormone treatment in a girl with Prader Willi syndrome.

dc.contributor.authorPandey, S Nen_US
dc.contributor.authorVaidya, R Aen_US
dc.contributor.authorIrani, Aen_US
dc.date.accessioned2003-04-10en_US
dc.date.accessioned2009-05-30T15:57:42Z
dc.date.available2003-04-10en_US
dc.date.available2009-05-30T15:57:42Z
dc.date.issued2003-04-10en_US
dc.description.abstractPrader Willi syndrome (PWS) is a rare endocrine-metabolic disorder that is characterised by neonatal hypotonia, hyperphagia, marked obesity, short stature, hypogonadism and behavioural problems. 7-20% percent of these children develop diabetes mellitus. A large number of individuals with PWS show growth hormone (GH) deficiency. Recent studies indicate beneficial effects of GH replacement therapy not only for their linear growth but also for correction of metabolic dysfunction. In the present communication this article details about the therapeutic outcome in a girl with PWS who received recombinant growth hormone (rGH), Genotropin. Some carry-over therapeutic benefits have been observed even after discontinuation of rGH.en_US
dc.description.affiliationBhavan's SPARC Center for Disorders of Growth & Puberty 13th N.S. Road, JVPD, Mumbai-400 049. bhaspa@bom5.vsnl.net.inen_US
dc.identifier.citationPandey SN, Vaidya RA, Irani A. Growth hormone treatment in a girl with Prader Willi syndrome. Indian Journal of Pediatrics. 2003 Apr; 70(4): 351-3en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/84115
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshAdolescenten_US
dc.subject.meshFemaleen_US
dc.subject.meshGlucose Tolerance Testen_US
dc.subject.meshGrowth --drug effectsen_US
dc.subject.meshHuman Growth Hormone --blooden_US
dc.subject.meshHumansen_US
dc.subject.meshPituitary Hormones, Anterior --blooden_US
dc.subject.meshPrader-Willi Syndrome --blooden_US
dc.subject.meshRecombinant Proteins --therapeutic useen_US
dc.subject.meshTreatment Outcomeen_US
dc.titleGrowth hormone treatment in a girl with Prader Willi syndrome.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
dc.typeResearch Support, Non-U.S. Gov'ten_US
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