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This symptom may arise through several mechanisms, including low blood glucose (hypoglycaemia), dehydration from gastrointestinal effects, orthostatic hypotension, or reduced caloric intake

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Prader-Willi syndrome (PWS) is a rare genetic disorder affecting approximately 1 in 15,000 births, characterized by severe hyperphagia (excessive hunger) that can lead to life-threatening obesity if left unmanaged

Taken together, SLC39A1/DRP1/MCU axis were critical for MMP reduction, mitochondrial fragmentation