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杰克逊检查表的再评估及两种唐氏综合征亚型的鉴定。

A reassessment of Jackson's checklist and identification of two Down syndrome sub-phenotypes.

机构信息

Neonatology Unit, St. Orsola-Malpighi Polyclinic, Via Massarenti 9, 40138, Bologna, BO, Italy.

Department of Developmental Psychology and Socialisation, University of Padova, Via Venezia 8, 35131, Padua, PD, Italy.

出版信息

Sci Rep. 2022 Feb 24;12(1):3104. doi: 10.1038/s41598-022-06984-0.

Abstract

Down syndrome (DS) is characterised by several clinical features including intellectual disability (ID) and craniofacial dysmorphisms. In 1976, Jackson and coll. identified a checklist of signs for clinical diagnosis of DS; the utility of these checklists in improving the accuracy of clinical diagnosis has been recently reaffirmed, but they have rarely been revised. The purpose of this work is to reassess the characteristic phenotypic signs and their frequencies in 233 DS subjects, following Jackson's checklist. 63.77% of the subjects showed more than 12 signs while none showed less than 5, confirming the effectiveness of Jackson's checklist for the clinical diagnosis of DS. An association between three phenotypic signs emerged, allowing us to distinguish two sub-phenotypes: Brachycephaly, short and broad Hands, short Neck (BHN), which is more frequent, and "non-BHN". The strong association of these signs might be interpreted in the context of the growth defects observed in DS children suggesting decreased cell proliferation. Lastly, cognitive assessments were investigated for 114 subjects. The lack of association between the presence of a physical sign or the number of signs present in a subject and cognitive skills disproves the stereotype that physical characteristics are predictive of degree of ID.

摘要

唐氏综合征(DS)的特征是包括智力障碍(ID)和颅面畸形在内的多种临床特征。1976 年,Jackson 等人确定了用于 DS 临床诊断的检查表;最近再次确认了这些检查表在提高临床诊断准确性方面的效用,但它们很少被修订。本研究的目的是根据 Jackson 的检查表重新评估 233 名 DS 患者的特征性表型体征及其频率。63.77%的患者表现出超过 12 种体征,而无一例患者表现出少于 5 种体征,这证实了 Jackson 检查表对 DS 临床诊断的有效性。三个表型体征之间存在关联,使我们能够区分两种亚表型:短头畸形、短而宽的手、短颈(BHN),其更为常见,另一种为“非-BHN”。这些体征的强关联可以在 DS 儿童中观察到的生长缺陷的背景下进行解释,表明细胞增殖减少。最后,对 114 名患者进行了认知评估。在一个患者中存在的物理体征的数量或存在的体征数量与认知技能之间缺乏关联,这否定了身体特征可以预测 ID 程度的刻板印象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9504/8873406/0f1abdd63f99/41598_2022_6984_Fig1_HTML.jpg

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