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Treatment of exenatide of Prader-Willi syndrome complicated with metabolic syndrome:a case report |
FANG Haining YU Fei▲ |
Pediatics Department of Endocrinology and Genetics Metabolism, Maternal and Child Health Care Hospital of Hubei Province,Wuhan 430070, China |
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Abstract Prader-Willi syndrome is a genomic imprinting disease that is highly susceptible to childhood and adolescence obesity, multiplex syndromes of metabolic syndrome such as hypertension, hyperglycemia and dyslipidemia due to overfeeding and obesity will seriously affect the survival rate and quality of life of children. In this paper, a case of genetically diagnosed 9 years old Prader-Willi syndrome child complicated with metabolic syndrome is reported to analyse the data of blood pressure, body weight, biochemistry, liver imaging and sleep apnea monitoring before and after treatment of human glucagon like peptide -1 receptor agonist-exenatide, this child's appetite decreased and the satiety increased, body weight and body mass index decreased, blood pressure decreased and stable in the normal range, low density lipoprotein cholesterol decreased, high density lipoprotein cholesterol increased, the CT value of the liver increased, apnea hypoventilation index decreased and tolerance was good after 6 months of exenatide treatment. This study provides a new possibility for the treatment of such children.
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