Introduction: A Practical Guide to Central Nervous System Malformations—From Genetics, to Diagnosis and Treatment

IF 0.2 Q4 PEDIATRICS Journal of pediatric neurology Pub Date : 2024-05-11 DOI:10.1055/s-0044-1786778
A. Praticò, A. Polizzi, Martino Ruggieri
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Abstract

Central nervous system (CNS) malformations encompass diverse congenital anomalies impacting brain and spinal cord development, profoundly affecting neurological function. They arise from disruptions in embryonic neural tube formation, neuronal migration, and cortical organization. This abstract provides a comprehensive overview of CNS malformations, covering classification, etiology, clinical manifestations, and diagnostic challenges. CNS malformations fall into distinct groups: neural tube defects (e.g., anencephaly, spina bifida), resulting from incomplete neural tube closure; malformations of cortical development (e.g., lissencephaly, polymicrogyria), featuring irregularities in cortical folding; and anomalies affecting structures like the corpus callosum, cerebellum, and CNS vasculature, alongside conditions such as hydrocephalus and Chiari malformations. Genetic factors, including mutations in LIS1, DCX, and RELN, contribute significantly, while environmental factors like maternal folic acid deficiency also play a role. Some malformations occur in genetic syndromes (e.g., tuberous sclerosis, neurofibromatosis). Clinical presentations vary, with neural tube defects typically presenting severe deficits at birth, while cortical malformations manifest as intellectual disabilities, seizures, and motor deficits. Hydrocephalus elevates intracranial pressure, and Chiari malformations cause headaches and neurological symptoms. Diagnosis necessitates a multidisciplinary approach involving clinical evaluation, neuroimaging, genetic testing, and histopathological analysis. Prenatal diagnosis via ultrasound and magnetic resonance imaging is crucial for planning interventions, while postnatal diagnosis relies on clinical and imaging findings.Understanding CNS malformations is vital for early detection, intervention, and comprehensive care provision. Advances in genetics and neuroimaging offer hope for improved outcomes and better quality of life for affected individuals.
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导言:中枢神经系统畸形实用指南--从遗传到诊断和治疗
中枢神经系统(CNS)畸形包括影响大脑和脊髓发育的各种先天性异常,严重影响神经功能。它们产生于胚胎神经管形成、神经元迁移和皮质组织的破坏。本摘要全面概述了中枢神经系统畸形,包括分类、病因、临床表现和诊断难题。中枢神经系统畸形分为不同组别:神经管闭合不全导致的神经管缺陷(如无脑畸形、脊柱裂);以皮质折叠不规则为特征的皮质发育畸形(如裂头畸形、多小脑畸形);影响胼胝体、小脑和中枢神经系统血管等结构的异常,以及脑积水和Chiari畸形等疾病。遗传因素(包括 LIS1、DCX 和 RELN 的突变)是导致畸形的主要原因,而环境因素(如母体叶酸缺乏)也起了一定作用。有些畸形发生在遗传综合征中(如结节性硬化症、神经纤维瘤病)。临床表现各不相同,神经管缺陷通常会在出生时表现出严重的缺陷,而皮质畸形则表现为智力障碍、癫痫发作和运动障碍。脑积水会使颅内压升高,而奇拉氏畸形则会引起头痛和神经症状。诊断需要采用多学科方法,包括临床评估、神经影像学检查、基因检测和组织病理学分析。通过超声波和磁共振成像进行产前诊断对于制定干预计划至关重要,而产后诊断则依赖于临床和成像结果。遗传学和神经影像学的进步为改善患者的预后和生活质量带来了希望。
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
52
期刊介绍: The Journal of Pediatric Neurology is a multidisciplinary peer-reviewed medical journal publishing articles in the fields of childhood neurology, pediatric neurosurgery, pediatric neuroradiology, child psychiatry and pediatric neuroscience. The Journal of Pediatric Neurology, the official journal of the Society of Pediatric Science of the Yüzüncü Yil University in Turkiye, encourages submissions from authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, rapid communications, case reports, neuroimage of the month, letters to the editor and book reviews.
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