Copes L E, Pober B R, Terilli C A
Department of Medical Sciences, Frank H. Netter MD School of Medicine, Quinnipiac University, Hamden, Connecticut.
Department of Genetics, Massachusetts General Hospital, Boston, Massachusetts.
Clin Anat. 2016 Jul;29(5):578-89. doi: 10.1002/ca.22685. Epub 2016 Jan 25.
Williams syndrome (WS), also referred to as Williams-Beuren syndrome (WBS), is a relatively rare genetic disorder affecting ∼1/10,000 persons. Since the disorder is caused by a micro-deletion of ∼1.5 Mb, it is not surprising that the manifestations of WS are extremely broad, involving most body systems. In this paper, we primarily focus on the musculoskeletal aspects of WS as these findings have not been the subject of a comprehensive review. We review the MSK features commonly seen in individuals with WS, along with related sensory and neurological issues interacting with and compounding underlying MSK abnormalities. We end by providing perspective, particularly from the vantage point of a physical therapist, on therapeutic interventions to address the most common MSK and related features seen in WS. Clin. Anat. 29:578-589, 2016. © 2016 Wiley Periodicals, Inc.
威廉姆斯综合征(WS),也被称为威廉姆斯-贝伦综合征(WBS),是一种相对罕见的遗传性疾病,发病率约为万分之一。由于该疾病是由约1.5兆碱基的微缺失引起的,因此WS的表现极为广泛,累及大多数身体系统也就不足为奇了。在本文中,我们主要关注WS的肌肉骨骼方面,因为这些发现尚未成为全面综述的主题。我们回顾了WS患者常见的肌肉骨骼特征,以及与潜在的肌肉骨骼异常相互作用并使其复杂化的相关感觉和神经问题。最后,我们从物理治疗师的角度提供了关于治疗干预的观点,以解决WS中最常见的肌肉骨骼及相关特征。《临床解剖学》2016年第29卷:578 - 589页。© 2016威利期刊公司。