首页> 外文期刊>Frontiers in Behavioral Neuroscience >Everyday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome trisomy (XXX and XXY)
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Everyday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome trisomy (XXX and XXY)

机译:唐氏综合症从幼儿期到成年后的日常执行功能:与具有性染色体三体性(XXX和XXY)的年轻人相比,具有独特和共同特征的证据

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Executive functions (EF) are thought to be impaired in Down syndrome (DS) and sex chromosome trisomy (Klinefelter and Trisomy X syndromes; +1X). However, the syndromic specificity and developmental trajectories associated with EF difficulties in these groups are poorly understood. The current investigation (a) compared everyday EF difficulties in youth with DS, +1X, and typical development (TD); and (b) examined relations between age and EF difficulties in these two groups and a TD control group cross-sectionally. Study 1 investigated the syndromic specificity of EF profiles on the Behavior Rating Inventory of Executive Function (BRIEF) in DS ( n = 30), +1X ( n = 30), and a TD group ( n = 30), ages 5–18 years. Study 2 examined age effects on EF in the same cross-sectional sample of participants included in Study 1. Study 3 sought to replicate Study 2's findings for DS by examining age-EF relations in a large independent sample of youth with DS ( n = 85) and TD ( n = 43), ages 4–24 years. Study 1 found evidence for both unique and shared EF impairments for the DS and +1X groups. Most notably, youth with +1X had relatively uniform EF impairments on the BRIEF scales, while the DS group showed an uneven BRIEF profile with relative strengths and weaknesses. Studies 2 and 3 provided support for fairly similar age-EF relations in the DS and TD groups. In contrast, for the +1X group, findings were mixed; 6 BRIEF scales showed similar age-EF relations to the TD group and 2 showed greater EF difficulties at older ages for +1X. These findings will be discussed within the context of efforts to identify syndrome specific cognitive-behavioral profiles for youth with different genetic syndromes in order to inform basic science investigations into the etiology of EF difficulties in these groups and to develop treatment approaches that are tailored to the needs of these groups.
机译:人们认为唐氏综合症(DS)和性染色体三体性(Klinefelter和Trisomy X综合征; + 1X)会损害执行功能(EF)。然而,这些人群中与EF困难相关的症状特异性和发展轨迹知之甚少。当前的调查(a)将DS,+ 1X和典型发展(TD)的年轻人日常EF困难进行了比较; (b)剖析了这两组和TD对照组的年龄和EF困难之间的关系。研究1研究了5至18岁的DS(n = 30),+ 1X(n = 30)和TD组(n = 30)在执行功能的行为评级清单(BRIEF)上EF谱的症状特异性。年份。研究2在研究1的参与者的同一横断面样本中检查了年龄对EF的影响。研究3通过检查大量独立于DS的青年(n = 85)中的年龄与EF关系,试图复制研究2的DS结果。 )和TD(n = 43),年龄为4-24岁。研究1发现了DS和+ 1X组独特和共同的EF损伤的证据。最显着的是,在BB量表上,具有+ 1X的青年人的EF损害相对均匀,而DS组则表现出不平衡的BB量表,具有相对的优势和劣势。研究2和3为DS和TD组中相当相似​​的年龄-EF关系提供了支持。相比之下,对于+ 1X组,发现结果好坏参半。 6简明量表显示出与TD组相似的年龄-EF关系,而2显示在+ 1X年龄较大的EF中难度更大。这些发现将在努力确定具有不同遗传综合征的年轻人的特定于综合征的认知行为特征的背景下进行讨论,以便为基础科学调查这些人群中EF困难的病因提供依据,并开发适合于这些人群的治疗方法这些群体的需求。

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