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首页> 外文期刊>The Journal of pediatrics >Specific cognitive deficits in young children with cystinosis: evidence for an early effect of the cystinosin gene on neural function.
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Specific cognitive deficits in young children with cystinosis: evidence for an early effect of the cystinosin gene on neural function.

机译:胱氨酸症幼儿的特殊认知缺陷:胱氨酸酶基因对神经功能的早期影响的证据。

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摘要

OBJECTIVES: Infantile nephropathic cystinosis is associated with a specific cognitive deficit in visual spatial processing in older children and adults. The cause of this deficit is unknown. This study was designed to determine whether the cognitive deficit is present in young children with cystinosis, suggesting an early effect of the genetic disorder on brain development. STUDY DESIGN: Young children (n = 25; age, 3-8 years) with cystinosis and 25 matched control subjects underwent cognitive testing, including tests of intelligence, visual perceptual, visual spatial, and visual motor functions. RESULTS: Children with cystinosis performed significantly more poorly on tests of visual spatial and visual motor function than did control subjects. Visual perceptual abilities were equivalent in the 2 groups. CONCLUSION: The same pattern of visual spatial deficit is present in young children with cystinosis as has previously been demonstrated in older children and adults, which suggests that there may be an influence of the cystinosis gene on brain development, rather than an adverse effect of prolonged cystine accumulation in the brain during childhood.
机译:目的:婴幼儿肾病性胱氨酸病与年龄较大的儿童和成人的视觉空间加工过程中的特定认知缺陷有关。这种赤字的原因尚不清楚。这项研究旨在确定在患有胱氨酸病的幼儿中是否存在认知缺陷,这表明遗传性疾病对大脑发育的早期影响。研究设计:患有胱氨酸病的幼儿(n = 25; 3-8岁)和25名相匹配的对照受试者接受了认知测试,包括智力,视觉知觉,视觉空间和视觉运动功能的测试。结果:与对照对象相比,胱氨酸病患儿在视觉空间和视觉运动功能测试中的表现明显较差。视觉感知能力在两组中相同。结论:与以前在较大的儿童和成人中发现的一样,在患有胱氨酸病的幼儿中存在相同的视觉空间缺陷模式,这表明胱氨酸病基因可能对大脑发育有影响,而不是长期的不良影响。儿童时期大脑中的胱氨酸积累。

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