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M. Kahssay

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Case report Open access Sep 2026

Child with genetically confirmed Prader-Willi syndrome

Summary Prader–Willi syndrome (PWS) is a rare genetic disorder caused by loss of paternal genes on chromosome 15. It is characterised by hyperphagia, obesity, endocrine deficiencies and neurodevelopmental challenges. We report on a boy in his early teens presenting with short stature, early-onset obesity and clinical f...

M. Kahssay, K. Oyieke, C. Høybye · 0 citations

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