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Inherited cerebellar ataxia in childhood: A pattern-recognition approach using brain MRI

机译:儿童遗传性小脑共济失调:使用脑MRI的模式识别方法

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Ataxia is the principal symptom of many common neurologic diseases in childhood. Ataxias caused by dysfunction of the cerebellum occur in acute, intermittent, and progressive disorders. Most of the chronic progressive processes are secondary to degenerative and metabolic diseases. In addition, congenital malformation of the midbrain and hindbrain can also be present, with posterior fossa symptoms related to ataxia. Brain MR imaging is the most accurate imaging technique to investigate these patients, and imaging abnormalities include size, shape, and/or signal of the brain stem and/or cerebellum. Supratentorial and cord lesions are also common. This review will discuss a pattern-recognition approach to inherited cerebellar ataxia in childhood. The purpose is to provide a comprehensive discussion that ultimately could help neuroradiologists better manage this important topic in pediatric neurology.
机译:共济失调是儿童许多常见神经系统疾病的主要症状。小脑功能障碍引起的共济失调发生在急性,间歇性和进行性疾病中。大多数慢性进行性过程是继发于变性和代谢性疾病的继发性疾病。此外,还可能存在中脑和后脑的先天性畸形,伴有共济失调的后颅窝症状。脑部MR成像是研究这些患者的最准确的成像技术,并且成像异常包括脑干和/或小脑的大小,形状和/或信号。幕上和脐带病变也很常见。本文将讨论儿童遗传性小脑共济失调的模式识别方法。目的是提供全面的讨论,最终可以帮助神经放​​射科医生更好地管理小儿神经病学中的这一重要主题。

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