Molecular Biology
Prader-Willi Syndrome (PWS) is a genetic disorder caused by the loss of function of specific genes on chromosome 15, leading to a range of physical, mental, and behavioral issues. Individuals with PWS typically exhibit hyperphagia, resulting in insatiable hunger, obesity, intellectual disabilities, and characteristic behavioral problems. This condition underscores the complexities of genetic disorders and inherited diseases, as it highlights how specific gene deletions can impact overall health and development.
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