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皮质发育障碍的遗传学

Genetics of disorders of cortical development.

作者信息

Gaitanis John N, Walsh Christopher A

机构信息

Neurology, Brown School of Medicine, Hasbro Children's Hospital, Providence, RI 02905, USA.

出版信息

Neuroimaging Clin N Am. 2004 May;14(2):219-29, viii. doi: 10.1016/j.nic.2004.03.007.

Abstract

Since the advent of MR imaging, cortical malformations have become an increasingly recognized cause of epilepsy and neurologic impairment. Improved radiographic characterization of cortical malformations has been requisite to defining their genetics, and a large portion of these disorders are now known to have a genetic basis. Uncovering genetic etiologies has provided insight into phenotypic diversity, revealed the importance of de novo mutations, and resulted in improved radiographic-genetic correlation. This article provides an overview of major cerebral cortical malformations and focuses on the genetic mechanisms of their causation.

摘要

自磁共振成像问世以来,皮质发育畸形已日益被认为是癫痫和神经功能障碍的一个病因。对皮质发育畸形进行更好的影像学特征描述对于确定其遗传学特征是必不可少的,现在已知这些疾病中有很大一部分具有遗传基础。揭示遗传病因有助于深入了解表型多样性,揭示新发突变的重要性,并提高影像学与遗传学的相关性。本文概述了主要的大脑皮质发育畸形,并着重介绍其发病的遗传机制。

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