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Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation

机译:巨头畸形,多微神经和带状带异位症:一种新的皮质畸形

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Megalencephalic polymicrogyria syndromes include megalencephaly-capillary malformation and megalencephaly-polymicro gyria-polydactyly-hydrocephalus. Recent genetic studies have identified that genes in the PI3K-AKT pathway are involved in the pathogenesis of these disorders. Herein, we report a patient who presented with developmental delay, epilepsy and peculiar neuroimaging findings of megalencephaly, polymicrogyria, and symmetrical band heterotopia in the periventricular region. The heterotopias exhibited inhomogeneous signals with undulatory mixtures of gray and white matter, resembling ribbon-like heterotopia, with a predominance in the temporal to occipital regions. These neuroradiological findings were not consistent with those in known megalencephalic polymicrogyria syndromes. No genetic abnormality was identified through whole-exome sequencing. The neuroimaging findings of this patient may represent a novel cortical malformation involving megalencephaly with polymicrogyria and ribbon-like band heterotopia. (C) 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
机译:巨脑性多小脑回综合征包括巨脑-毛细血管畸形和巨脑-多微回-多发性脑积水。最近的遗传研究已经确定,PI3K-AKT途径中的基因与这些疾病的发病机制有关。在本文中,我们报道了一名患者,其脑室周围区域出现发育迟缓,癫痫和特殊的神经影像学发现,包括巨头畸形,多微神经和对称带状异位症。异位症在灰色和白色物质的波动混合物中表现出不均匀的信号,类似于带状异位症,主要在颞部到枕骨区域。这些神经放射学发现与已知的大脑多微神经综合征的发现不一致。通过全外显子组测序未发现遗传异常。该患者的神经影像学表现可能代表了一种新的皮质畸形,包括巨头畸形伴有多小神经和带状带异位症。 (C)2016年日本儿童神经病学会。由Elsevier B.V.发布。保留所有权利。

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