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首页> 外文期刊>Acta Radiologica >White matter abnormalities in children with idiopathic developmental delay.
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White matter abnormalities in children with idiopathic developmental delay.

机译:特发性发育迟缓儿童的白质异常。

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摘要

BACKGROUND: The underlying cause of developmental delay (DD) often remains unclear despite extensive clinical examination and investigations. Interference in normal development of the brain may result in DD. PURPOSE: To identify the prevalence of abnormalities on magnetic resonance (MR) imaging in idiopathic developmental delay. MATERIAL AND METHods: Of the 124 children referred for MR imaging with DD, 34 were excluded due to known history of progressive neurodevelopmental disorders, birth asphyxia, congenital CNS infections, metabolic disorder, chromosomal anomalies, and severe epileptic syndromes. The following structures were systematically reviewed: ventricles, corpus callosum, gray and white matter, limbic system, basal ganglia, brainstem, and cerebellum. RESULTS: Ten out of 90 (11%) were referred with DD only, whilst 80/90 (89%) were referred with DD and additional clinical findings, such as seizures, neurological deficit, and abnormal head size. Of the 90 patients, 14 (16%) had normal MR and 76 (84%) had abnormal MR findings. Abnormal ventricles were seen in 43/90 (48%); abnormal corpus callosum was identified in 40/90 (44%). Other MR findings included abnormalities in the white matter (23/90, 26%), hippocampi (5/90, 6%), cerebellum (5/90, 6%), and brainstem (4/90, 4%). CONCLUSION: Abnormalities of the ventricles and corpus callosum were identified in a large proportion of patients with idiopathic DD, indicative of changes in the white matter. Further studies using quantitative methods and diffusion tensor imaging are required to evaluate the white matter in these children.
机译:背景:尽管进行了广泛的临床检查和研究,但发育迟缓(DD)的根本原因通常仍不清楚。干扰大脑的正常发育可能会导致DD。目的:确定在特发性发育延迟中磁共振(MR)成像异常的患病率。材料和方法:由于已知的进行性神经发育障碍,出生窒息,先天性中枢神经系统感染,代谢异常,染色体异常和严重的癫痫综合症的病史,在124位接受DD MR成像的儿童中,有34位被排除在外。系统地审查了以下结构:脑室,体,灰色和白色物质,边缘系统,基底神经节,脑干和小脑。结果:90名患者中有10名(11%)仅接受DD,而80/90名患者(89%)具有DD和其他临床发现,例如癫痫发作,神经功能缺损和头部异常。在90例患者中,MR正常的14例(16%),MR异常的76例(84%)。观察到心室异常(43/90)(48%);在40/90(44%)中发现异常体。其他MR发现包括白质异常(23/90,26%),海马(5/90,6%),小脑(5/90,6%)和脑干(4/90,4%)异常。结论:在大部分特发性DD患者中发现了脑室和call体异常,表明白质发生了变化。需要使用定量方法和扩散张量成像的进一步研究来评估这些儿童的白质。

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