Neurocrine Biosciences· @neurocrine · X·· 2026-06-30AI 评分3
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你听说过 Prader-Willi 综合征吗？ PWS 是一种罕见的遗传性神经发育障碍，影响身体多个系统。 对于 PWS 患者，症状可包括发育迟缓、行为挑战和食欲亢进——后者是一种标志性特征，表现为持续无法通过食物满足的饥饿感。 提高认知与教育有助于增进对 PWS 患者的理解。 了解更多请访问 http://support4pws.com/ #PWSAwareness #Support4PWS
正文
Have you heard of Prader-Willi syndrome?
PWS is a rare genetic neurodevelopmental disorder that affects multiple systems in the body.
For those living with PWS, symptoms can include developmental delays, behavioral challenges and hyperphagia, a defining feature characterized by a persistent sensation of hunger that cannot be satisfied with food.
Awareness and education support greater understanding for individuals living with PWS.
Learn more at http://support4pws.com/
#PWSAwareness #Support4PWS
来源：Neurocrine Biosciences · x.com