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本文引用的文献

1
Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.《Phelan-McDermid 综合征的临床和遗传方面:管理的跨学科方法》
Genes (Basel). 2022 Mar 12;13(3):504. doi: 10.3390/genes13030504.
2
Phelan-McDermid syndrome: a classification system after 30 years of experience.佩兰-麦克德米德综合征:30 年经验后的分类系统。
Orphanet J Rare Dis. 2022 Jan 29;17(1):27. doi: 10.1186/s13023-022-02180-5.
3
Characterisation of the clinical phenotype in Phelan-McDermid syndrome.佩兰-麦克德米德综合征的临床表型特征。
J Neurodev Disord. 2021 Jul 10;13(1):26. doi: 10.1186/s11689-021-09370-5.
4
Correction: Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome.更正:费兰-麦克德米德(22q13.3)综合征的言语和语言表型
Eur J Hum Genet. 2021 Apr;29(4):719. doi: 10.1038/s41431-021-00855-4.
5
[Prevalence of the Phelan-McDermid Syndrome in Spain.].[西班牙费兰-麦克德米德综合征的患病率。]
Rev Esp Salud Publica. 2020 Dec 21;94:e202012121.
6
A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.一个由 29 名中国大陆患者组成的 Phelan-McDermid 综合征队列:基因型-表型相关性以及 SHANK3 杂合不足在重要表型中的作用。
Orphanet J Rare Dis. 2020 Nov 30;15(1):335. doi: 10.1186/s13023-020-01592-5.
7
Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome.费兰-麦克德米德综合征的发育、沟通及行为深度表型分析
Mol Syndromol. 2020 Jan;10(6):294-305. doi: 10.1159/000503840. Epub 2019 Nov 5.
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9
Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome.评估与严重智力和多重残疾(PIMD)相关的罕见遗传性疾病个体的框架:以 Phelan-McDermid 综合征为例。
Clin Neuropsychol. 2018 Aug-Oct;32(7):1226-1255. doi: 10.1080/13854046.2017.1413211. Epub 2017 Dec 21.
10
Prospective study of autism phenomenology and the behavioural phenotype of Phelan-McDermid syndrome: comparison to fragile X syndrome, Down syndrome and idiopathic autism spectrum disorder.前瞻性研究孤独症表型和 Phelan-McDermid 综合征的行为表型:与脆性 X 综合征、唐氏综合征和特发性孤独症谱系障碍的比较。
J Neurodev Disord. 2017 Nov 10;9(1):37. doi: 10.1186/s11689-017-9217-6.

费兰-麦克德米德综合征和自闭症谱系障碍中适应性行为的描述性分析

Descriptive Analysis of Adaptive Behavior in Phelan-McDermid Syndrome and Autism Spectrum Disorder.

作者信息

Serrada-Tejeda Sergio, Martínez-Piédrola Rosa M, Máximo-Bocanegra Nuria, Sánchez-Herrera-Baeza Patricia, Pérez-de-Heredia-Torres Marta

机构信息

Department of Physical Therapy, Occupational Therapy, Rehabilitation and Physical Medicine, Rey Juan Carlos University, Madrid, Spain.

出版信息

Front Neurosci. 2022 Jul 4;16:893003. doi: 10.3389/fnins.2022.893003. eCollection 2022.

DOI:10.3389/fnins.2022.893003
PMID:35864987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9295709/
Abstract

INTRODUCTION

The variety in symptomatology and clinical presentation of individuals diagnosed with Phelan-McDermid Syndrome (PMS) can delay medical diagnosis, so identifying specific neurobehavioral variables and facilitating differential diagnosis with patients with idiopathic Autism Spectrum Disorder (ASD) can guide early detection.

METHODS

A descriptive analysis of the level of adaptive behavior in 50 patients diagnosed with PMS was performed ( : = 44 : = 6). Subsequently, a comparative analysis was performed with 28 children aged between 4 years and 6 years and 11 months ( = 14; ASD = 14). Differences between the two groups were evaluated and Bonferroni correction was applied for multiple comparisons.

RESULTS

Differences were identified in the variables of communication ( = -2.715, = 0.007), Self-Direction ( = -2.199, = 0.028) and social participation ( = -3.190, = 0.001), with better adaptive behavior skills being observed in participants with a SHANK3 . Better adaptive skills in the sample of participants with , were found and statistically significant differences were identified in the variables of academic skills ( = -3.084, = 0.002), use of community resources ( = -1.889, = 0.050) and health and safety ( = -2.90, = 0.004).

CONCLUSION

Participants with show better communication and social participation skills than those with a diagnosis of . The observed differences between ASD and individuals with PMS reflect deficits in practical and conceptual adaptive skills that may limit and hinder daily adaptive functioning.

摘要

引言

被诊断为费兰-麦克德米德综合征(PMS)的个体在症状学和临床表现上存在差异,这可能会延迟医学诊断,因此识别特定的神经行为变量并促进与特发性自闭症谱系障碍(ASD)患者的鉴别诊断可以指导早期检测。

方法

对50例被诊断为PMS的患者的适应性行为水平进行了描述性分析(男=44;女=6)。随后,对28名年龄在4岁至6岁11个月之间的儿童进行了比较分析(典型发育=14;ASD=14)。评估了两组之间的差异,并应用邦费罗尼校正进行多重比较。

结果

在沟通(t=-2.715,p=0.007)、自我导向(t=-2.199,p=0.028)和社会参与(t=-3.190,p=0.001)变量中发现了差异,在携带SHANK3突变的参与者中观察到更好的适应性行为技能。在携带突变的参与者样本中发现了更好的适应技能,并且在学术技能(t=-3.084,p=0.002)、社区资源利用(t=-1.889,p=0.050)和健康与安全(t=-2.90,p=0.004)变量中发现了统计学上的显著差异。

结论

携带SHANK3突变的参与者比被诊断为ASD的参与者表现出更好的沟通和社会参与技能。观察到的ASD与PMS个体之间的差异反映了实践和概念适应性技能的缺陷,这可能会限制和阻碍日常适应性功能。