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Published in 2022 at "Nutrients"
DOI: 10.3390/nu14040860
Abstract: Prader–Willi Syndrome (PWS) is a human genetic condition that affects up to 1 in 10,000 live births. Affected infants present with hypotonia and developmental delay. Hyperphagia and increasing body weight follow unless drastic calorie restriction…
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Keywords:
prader willi;
snord116m;
body weight;
willi syndrome ... See more keywords