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本文引用的文献

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Vax1, a novel homeobox-containing gene, directs development of the basal forebrain and visual system.Vax1是一种新型的含同源盒基因,指导基底前脑和视觉系统的发育。
Genes Dev. 1999 Dec 1;13(23):3106-14. doi: 10.1101/gad.13.23.3106.
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Partial midline fusion of the cerebellar hemispheres with vertical folia: a new cerebellar malformation?小脑半球部分中线融合伴垂直小叶:一种新的小脑畸形?
AJNR Am J Neuroradiol. 1999 Jun-Jul;20(6):1151-3.
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Rostral vermian cortical dysplasia: MRI.延髓嘴侧皮质发育异常:磁共振成像
Neuroradiology. 1999 Mar;41(3):190-4. doi: 10.1007/s002340050732.
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Neuroimaging manifestations and classification of congenital muscular dystrophies.先天性肌营养不良的神经影像学表现及分类
AJNR Am J Neuroradiol. 1998 Sep;19(8):1389-96.
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MR of cerebellar cortical dysplasia.小脑皮质发育异常的磁共振成像
AJNR Am J Neuroradiol. 1998 May;19(5):984-6.
6
Analysis of aberrant neuronal migrations in the hereditary cerebellar vermis defect (CVD) rat using bromodeoxyuridine immunohistochemistry.利用溴脱氧尿苷免疫组织化学法分析遗传性小脑蚓部缺损(CVD)大鼠中异常的神经元迁移。
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Chronological and immunohistochemical observations of cerebellar dysplasia and vermis defect in the hereditary cerebellar vermis defect (CVD) rat.遗传性小脑蚓部缺损(CVD)大鼠小脑发育异常和蚓部缺损的时间顺序及免疫组织化学观察
Acta Neuropathol. 1997 Dec;94(6):549-56. doi: 10.1007/s004010050749.
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Genetic disorders and cerebellar structural abnormalities in childhood.儿童期的遗传疾病和小脑结构异常
Brain. 1997 Oct;120 ( Pt 10):1739-51. doi: 10.1093/brain/120.10.1739.
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Macrocerebellum: neuroimaging and clinical features of a newly recognized condition.巨小脑:一种新发现病症的神经影像学及临床特征
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MR demonstration of cerebral hemimegalencephaly associated with cerebellar involvement (total hemimegalencephaly).大脑半球巨脑畸形合并小脑受累(全大脑半球巨脑畸形)的磁共振成像表现
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小脑皮质发育异常:复杂病变的磁共振成像表现

Cerebellar cortical dysplasia: MR findings in a complex entity.

作者信息

Soto-Ares G, Delmaire C, Deries B, Vallee L, Pruvo J P

机构信息

Department of Neuroradiology, Hôpital Roger Salengro, Chru Lille France.

出版信息

AJNR Am J Neuroradiol. 2000 Sep;21(8):1511-9.

PMID:11003288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7974055/
Abstract

BACKGROUND AND PURPOSE

MR imaging findings of cerebellar cortical dysplasia have been described as a new cerebellar malformation. The purpose of this study was to assess the association of cerebellar cortical dysplasia with other cerebral malformations.

METHODS

We retrospectively reviewed 46 MR examinations of patients presenting with developmental delay, hypotonia, and facial deformities to identify abnormal folia or fissures or both within cerebellar hemispheres or vermis suggesting cortical dysplasia.

RESULTS

Cerebellar cortical dysplasia was diagnosed in 17 patients. In two patients, it was isolated. In the remaining 15 patients, the malformation was associated with vermian malformation (n=11), cerebral cortical dysplasias (n=8), dysplasia of corpus callosum (n=6), and heterotopia (n=5). A widespread malformation of the posterior fossa was observed in eight patients (Dandy-Walker, Chiari II and III, and hypoplasia of brain stem). One patient with hypertrophied cerebellar hemisphere had minor enlargement of the right cerebral hemisphere and lateral ventricle. He also had nodular heterotopia, suggesting unilateral megalencephaly.

CONCLUSION

Our study suggests that cerebellar cortical dysplasias are common in cases with more widespread cerebral malformations. Technical progress providing high-quality tridimensional MR imaging of the cerebellum may explain its recent descriptions.

摘要

背景与目的

小脑皮质发育异常的磁共振成像表现已被描述为一种新的小脑畸形。本研究的目的是评估小脑皮质发育异常与其他脑畸形的关联。

方法

我们回顾性分析了46例发育迟缓、肌张力减退和面部畸形患者的磁共振检查,以确定小脑半球或蚓部内提示皮质发育异常的异常小叶或裂隙或两者皆有。

结果

17例患者被诊断为小脑皮质发育异常。其中2例为孤立性病变。其余15例患者中,该畸形与蚓部畸形(n = 11)、大脑皮质发育异常(n = 8)、胼胝体发育异常(n = 6)和异位(n = 5)相关。8例患者观察到广泛的后颅窝畸形(丹迪-沃克畸形、Chiari II和III型以及脑干发育不全)。1例小脑半球肥大患者右侧大脑半球和侧脑室轻度增大。他还患有结节性异位,提示单侧巨脑症。

结论

我们的研究表明,小脑皮质发育异常在更广泛的脑畸形病例中很常见。提供高质量小脑三维磁共振成像的技术进步可能解释了其最近才被描述的原因。