Glucagon like pepetide-1 agonist in a patient with prader-willi syndrome: a Sri Lankan experience

<p><strong>Background</strong></p><p>Prader-Willi Syndrome (PWS) is a genetic disease characterized by morbid obesity and hyperphagia. Although the exact pathophysiological basis of obesity and hyperphagia remains unclear it is thought to be mainly due to hypothalamic d...

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Bibliographic Details
Main Authors: Maulee Hiromi Arambewela, Noel P. Somasundaram
Format: Article
Language:English
Published: Sri Lanka College of Endocrinologists 2017-10-01
Series:Sri Lanka Journal of Diabetes Endocrinology and Metabolism
Subjects:
Online Access:https://sjdem.sljol.info/articles/7337