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J Inherit Metab Dis. 2011 Jun;34(3):711-21. doi: 10.1007/s10545-011-9318-4. Epub 2011 Apr 14.
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Brain MRI findings in patients with Fabry disease.脑 MRI 在法布里病患者中的表现。
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A case of adult-onset type II citrullinemia with comorbid epilepsy even after liver transplantation.成年起病型 II 型瓜氨酸血症伴发癫痫,即使在肝移植后仍存在。
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Teaching NeuroImages: neuroimaging leads to recognition of previously undiagnosed Fabry disease.教学神经影像:神经影像学检查促使识别出先前未被诊断出的法布里病。
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Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency.弥散张量成像检测到部分鸟氨酸转氨甲酰酶缺乏症患者的白质微观结构异常区域。
AJNR Am J Neuroradiol. 2010 Oct;31(9):1719-23. doi: 10.3174/ajnr.A2122. Epub 2010 May 20.
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Brain imaging in urea cycle disorders.脑成像在尿素循环障碍中的应用。
Mol Genet Metab. 2010;100 Suppl 1(Suppl 1):S20-30. doi: 10.1016/j.ymgme.2010.01.017. Epub 2010 Feb 13.
7
Age-related decline in the microstructural integrity of white matter in children with early- and continuously-treated PKU: a DTI study of the corpus callosum.年龄相关的儿童早发性和持续性苯丙酮尿症患者白质微观结构完整性下降:胼胝体的弥散张量成像研究。
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Disruption of prefrontal function and connectivity in individuals with phenylketonuria.苯丙酮尿症患者前额叶功能和连接的中断。
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Executive function in early-treated phenylketonuria: profile and underlying mechanisms.早期治疗苯丙酮尿症患者的执行功能:特征及潜在机制。
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Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts.精氨酸酶缺乏症的弥散张量成像显示皮质脊髓束损伤。
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神经影像学在先天性代谢错误中的新应用。

New frontiers in neuroimaging applications to inborn errors of metabolism.

机构信息

Department of Neurology, Children's National Medical Center, Washington, D.C. 20010, USA.

出版信息

Mol Genet Metab. 2011 Nov;104(3):195-205. doi: 10.1016/j.ymgme.2011.06.020. Epub 2011 Jun 30.

DOI:10.1016/j.ymgme.2011.06.020
PMID:21778100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3758691/
Abstract

Most inborn errors of metabolism (IEMs) are associated with potential for injury to the developing central nervous system resulting in chronic encephalopathy, though the etiopathophysiology of neurological injury have not been fully established in many disorders. Shared mechanisms can be envisioned such as oxidative injury due to over-activation of N-Methyl-d-Aspartate (NMDA) receptors with subsequent glutamatergic damage, but other causes such as energy depletion or inflammation are possible. Neuroimaging has emerged as a powerful clinical and research tool for studying the brain in a noninvasive manner. Several platforms exist to study neural networks underlying cognitive processes, white matter/myelin microstructure, and cerebral metabolism in vivo. The scope and limitations of these methods will be discussed in the context of valuable information they provide in the study and management of selected inborn errors of metabolism. This review is not meant to be an exhaustive coverage of diagnostic findings on MRI in multiple IEMs, but rather to illustrate how neuroimaging modalities beyond T1 and T2 images, can add depth to an understanding of the underlying brain changes evoked by the selected IEMs. Emphasis will be placed on techniques that are available in the clinical setting. Though technically complex, many of these modalities have moved - or soon will - to the clinical arena.

摘要

大多数先天性代谢缺陷(IEMs)都与潜在的中枢神经系统发育损伤有关,导致慢性脑病,尽管许多疾病的神经损伤的病因和发病机制尚未完全确定。可以设想一些共同的机制,如 NMDA 受体过度激活引起的氧化损伤,随后发生谷氨酸能损伤,但也可能有其他原因,如能量耗竭或炎症。神经影像学已成为一种强大的临床和研究工具,用于非侵入性地研究大脑。目前有几种平台可用于研究认知过程、白质/髓鞘微观结构和体内大脑代谢的神经网络。将讨论这些方法的范围和局限性,以及它们在选定的先天性代谢缺陷的研究和管理中提供的有价值的信息。本综述并非旨在全面涵盖多种先天性代谢缺陷的 MRI 诊断结果,而是旨在说明 T1 和 T2 图像以外的神经影像学方式如何深入了解所选先天性代谢缺陷引起的潜在脑变化。重点将放在临床环境中可用的技术上。尽管技术上很复杂,但其中许多方式已经或即将进入临床领域。