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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >CORTICAL PENCIL LINING IN NEUROFERRITINOPATHY: A DIAGNOSTIC CLUE
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CORTICAL PENCIL LINING IN NEUROFERRITINOPATHY: A DIAGNOSTIC CLUE

机译:皮质铅笔NEUROFERRITINOPATHY衬里:A诊断线索

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摘要

Neurodegeneration with brain iron accumulation (NBIA) includes pantothenate kinase-associated neurodegeneration (PKAN, NBIA1), PLA2G6-associated neurodegeneration (PLAN, NBIA2), neuroferritinopathy, aceruloplasminemia, and MIN-associated neurodegeneration (MPAN).(1) Clinically, they can have similar presentation, with a combination of progressive extrapyramidal, cognitive, and bulbar features.(1) Since genetic testing is costly and not easily accessible, MRI clues, such as the eye of the tiger sign for PKAN,(2,3) are useful to guide the confirmatory genetic analyses. Herein, we describe a distinct imaging pattern of cortical iron deposition on susceptibility-weighted MRI (SWI) in genetically proven cases of neuroferritinopathy, which is not seen in genetically proven cases of PKAN or PLAN, the 2 most common forms of NBIA.
机译:神经退化与脑铁沉积(答案)包括泛酸盐kinase-associatedPLA2G6-associated神经退化(计划,和MIN-associated神经退化(MPAN)。(1)临床上,他们可以有类似的演讲中,的进步锥体束外的,认知和球特性。(1)因为遗传测试是昂贵和不方便,核磁共振线索,比如老虎的眼睛的迹象PKAN(2、3)是有用的指导确认遗传分析。成像的皮质铁沉积模式susceptibility-weighted MRI(瑞士)的基因证明neuroferritinopathy病例,这不是在基因证明PKAN或计划的情况下,答案的两个最常见的形式。

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