Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome
Abstract
Prader-Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resulting from the absence of expression of a group of genes on the paternally acquired chromosome 15q11-q13. Phenotypical characteristics of PWS include infantile hypotonia, short stature, incomplete pubertal development, hyperphagia and morbid obesity. Hypothalamic dysfunction in controlling body weight and food intake is a hallmark of PWS. Neuroimaging...
Paper Details
Title
Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome
Published Date
Jun 22, 2021
Volume
33
Issue
7
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