Screening Procedure for Hemihypertrophy: Preliminary Results of International Multicenter Prospective Study

M. Vaiman, Phillip Shilco, Yulia Roitblat, N. Padilla-Raygoza, Aidan Leit, A. Kavin, Edan Schonberger, Liliia Nehuliaieva, Noa Buchris, M. Shterenshis
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Abstract

Introduction Isolated or congenital hemihypertrophy is a rare disorder characterized by asymmetric overgrowth of one side of the body. This article describes the protocol and preliminary results of a lateral body asymmetry (hemihypertrophy) screening procedure performed in healthy adolescents in a multicenter study. The reported incidence of hemihypertrophy varies between different publications and standardized protocols are needed to improve research in this area. Methods Our screening program is taking place in Australia, Israel, Mexico, Ukraine and USA. Procedure includes two steps: (1) “three measurements – three questions” screening, or assessment of face, palms, and shins; (2) in-depth assessment of selected cases in order to exclude localized, lesional, and syndrome-related cases as well as body asymmetry within normative range and to select suspected cases of isolated hemihypertrophy. This step includes measurements of various anatomical regions and a detailed questionnaire. Results At this stage, the screening procedure is completed and the selected participants are advised to refer to medical institutions for further clinical and genetic follow up to exclude possible tumors and other accompanying disorders. Conclusion We present an easy-to-use selection tool to identify children with suspected IH, which results in the selection of the risk group that may benefit from referral to a pediatrician and a clinical geneticist.
半肥厚症的筛选程序:国际多中心前瞻性研究的初步结果
引言孤立性或先天性偏侧肥大是一种罕见的疾病,其特征是一侧身体不对称过度生长。本文描述了在一项多中心研究中对健康青少年进行的侧体不对称(偏侧肥大)筛查程序的方案和初步结果。报道的偏侧肥大的发生率在不同的出版物中有所不同,需要标准化的方案来改进这一领域的研究。方法我们的筛查项目在澳大利亚、以色列、墨西哥、乌克兰和美国进行。程序包括两个步骤:(1)“三项测量-三个问题”筛查,或评估面部、手掌和胫骨;(2) 对所选病例进行深入评估,以排除规范范围内的局限性、病变性和综合征相关病例以及身体不对称,并选择孤立性偏侧肥大的疑似病例。该步骤包括对不同解剖区域的测量和详细的问卷调查。结果在这个阶段,筛查程序已经完成,建议选定的参与者去医疗机构进行进一步的临床和基因随访,以排除可能的肿瘤和其他伴随疾病。结论我们提供了一种易于使用的选择工具来识别疑似IH儿童,从而选择可能受益于转诊至儿科医生和临床遗传学家的风险群体。
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来源期刊
Central Asian Journal of Global Health
Central Asian Journal of Global Health PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
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