Prader-Willi Syndrome: The More We Know, the Less We Know.

Missouri medicine Pub Date : 2024-05-01
Barbara Y Whitman
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引用次数: 0

Abstract

Prader-Willi syndrome (PWS) is a complex genetic neurodevelopmental disorder with multisystem impact and a unique behavior profile that evolves over the life span. Beyond the primary care needs of all children and adults, the unique medical concerns and management needs of those with PWS are best served in a multidisciplinary academic center. Our PWS center has provided care for individuals with PWS and their families since 1981. Our growth hormone studies contributed to growth hormone supplementation becoming standard of care in this country. Here, in collaboration with the primary care provider, early childhood intervention programs, schools and local parent organizations, solid, patient-centered care for affected individuals and their families can be provided across the life-span. The purpose of this article is to provide a brief overview of PWS and the attendant medical and behavior management challenges attendant to the disorder.

普拉德-威利综合征:我们知道的越多,了解的越少。
普拉德-威利综合征(PWS)是一种复杂的遗传性神经发育障碍,会对多个系统产生影响,其独特的行为特征会在人的一生中不断演变。除了满足所有儿童和成人的基本医疗需求外,PWS 患者的独特医疗问题和管理需求最好由多学科学术中心来解决。自 1981 年以来,我们的 PWS 中心一直为 PWS 患者及其家庭提供医疗服务。我们的生长激素研究促使生长激素补充成为美国的标准治疗方法。在这里,通过与初级保健提供者、儿童早期干预项目、学校和当地家长组织的合作,可以为受影响的患者及其家庭提供贯穿整个生命周期的、以患者为中心的可靠护理。本文旨在简要介绍 PWS 以及随之而来的医疗和行为管理方面的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
0.00%
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0
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