唐综合征患儿关节活动范围正常。

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY
Jordan T Jones, Nasreen Talib, Emily Cramer, Meg E Gasparovich, Elizabeth N Schroeder, Matthew McLaughlin, Jacqueline Kitchen
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引用次数: 0

摘要

唐氏综合症是导致智力残疾的最常见的染色体疾病之一。患有DS的儿童有许多不同的炎症和非炎症条件,这些条件会影响关节活动性,导致关节痛和关节活动范围(ROM)改变,因此,有正常的参考值进行比较以确定损伤程度是很重要的。本研究的目的是使用标准化测量方法,为患有DS的男女健康儿童的上下关节建立标准的关节ROM值。本研究评估了先前没有肌肉骨骼病理的患有DS的健康男性和女性的关节ROM。年轻的男性比同龄的女性有更多的ROM,而且随着年龄的增长,两性的ROM都会减少,但与没有DS的儿童相比,脚踝的ROM仍然增加。这项研究建立了DS儿童关节ROM的最佳估计值,当评估需要评估关节ROM以了解评估是否在正常ROM范围内时,这些信息应该有助于临床医生。这一参考应该有利于跟踪关节疾病随时间的进展,或者作为DS儿童关节ROM异常的肌肉骨骼筛查的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Normal joint range of motion in children with Down syndrome.

Down syndrome (DS) is one of the most common chromosomal conditions that results in intellectual disability. Children with DS have many different inflammatory and noninflammatory conditions that can affect joint mobility leading to arthralgia and altered joint range of motion (ROM), and it is important to have normal reference values for comparison to determine the degree of impairment. The objective of this study was to establish normative joint ROM values, using a standardized measurement approach, for upper and lower joints of healthy children of both genders with DS. This study evaluated joint ROM in healthy males and females with DS who had no previous musculoskeletal pathology. Younger males have more ROM than females at the same age and both genders lose ROM with age but continue to have increased ROM in the ankles compared to children without DS. This study establishes optimal estimates of joint ROM in children with DS, and this information should be helpful to clinicians when assessment requires evaluation of joint ROM to know if evaluation falls within the normal ROM. This reference should be helpful to track joint disease progression over time or as part of a musculoskeletal screen for abnormal joint ROM in children with DS.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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