脑海绵状血管瘤的流行病学和病因学。

Q2 Medicine
Hiroki Hongo, Satoru Miyawaki, Nobuhito Saito
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引用次数: 0

摘要

脑海绵体畸形(CCMs)是影响中枢神经系统的血管异常,发生率高达0.5%。这些病变的特点是薄壁血管扩张,易出血。它们可引起几种症状,如癫痫发作、出血性中风和局灶性神经功能缺损。临床研究揭示了CCMs的流行病学和自然史。人类遗传学研究已经确定了CCM1、CCM2和CCM3为已建立的驱动基因,最近,PIK3CA和MAP3K3被确定为额外的潜在驱动基因。此外,在遗传信息的基础上,动物研究已经开发出模型生物,包括小鼠模型,高度概括了人类CCMs,促进了分子机制的阐明。本文简要介绍了CCMs的流行病学和病因学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology and Aetiology of Cerebral Cavernous Malformations.

Cerebral cavernous malformations (CCMs) are vascular anomalies affecting the central nervous system in up to 0.5% of the population. These lesions are characterised by thin-walled, dilated blood vessels that are susceptible to haemorrhage. They can cause several symptoms, such as epileptic seizures, haemorrhagic strokes, and focal neurological deficits. Clinical studies have revealed the epidemiology and natural history of CCMs. Human genetic studies have identified CCM1, CCM2, and CCM3 as established driver genes, and more recently, PIK3CA and MAP3K3 have been identified as additional potential driver genes. Moreover, on the basis of genetic information, animal studies have developed model organisms, including murine models, that highly recapitulate human CCMs, facilitating the elucidation of molecular mechanisms. This article provides a brief overview of the epidemiology and aetiology of CCMs.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
2
期刊介绍: In addition to the regular journal, "Acta Neurochirurgica" publishes 3-4 supplement volumes per year. These comprise proceedings of international meetings or other material of general neurosurgical interest.
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