Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands.
Nat Rev Neurol. 2020 Nov;16(11):618-635. doi: 10.1038/s41582-020-0395-6. Epub 2020 Sep 7.
Malformations of cortical development (MCDs) are neurodevelopmental disorders that result from abnormal development of the cerebral cortex in utero. MCDs place a substantial burden on affected individuals, their families and societies worldwide, as these individuals can experience lifelong drug-resistant epilepsy, cerebral palsy, feeding difficulties, intellectual disability and other neurological and behavioural anomalies. The diagnostic pathway for MCDs is complex owing to wide variations in presentation and aetiology, thereby hampering timely and adequate management. In this article, the international MCD network Neuro-MIG provides consensus recommendations to aid both expert and non-expert clinicians in the diagnostic work-up of MCDs with the aim of improving patient management worldwide. We reviewed the literature on clinical presentation, aetiology and diagnostic approaches for the main MCD subtypes and collected data on current practices and recommendations from clinicians and diagnostic laboratories within Neuro-MIG. We reached consensus by 42 professionals from 20 countries, using expert discussions and a Delphi consensus process. We present a diagnostic workflow that can be applied to any individual with MCD and a comprehensive list of MCD-related genes with their associated phenotypes. The workflow is designed to maximize the diagnostic yield and increase the number of patients receiving personalized care and counselling on prognosis and recurrence risk.
皮质发育障碍(MCD)是一种神经发育障碍,源于宫内大脑皮质的异常发育。MCD 给受影响的个人、他们的家庭和全世界的社会带来了巨大的负担,因为这些人可能会经历终身耐药性癫痫、脑瘫、进食困难、智力残疾和其他神经和行为异常。由于临床表现和病因广泛存在差异,MCD 的诊断途径较为复杂,从而阻碍了及时和充分的管理。在本文中,国际 MCD 网络 Neuro-MIG 提供了共识建议,以帮助专家和非专家临床医生对 MCD 进行诊断,旨在改善全球患者的管理。我们回顾了主要 MCD 亚型的临床表现、病因和诊断方法的文献,并收集了来自 Neuro-MIG 临床医生和诊断实验室的当前实践和建议的数据。我们使用专家讨论和 Delphi 共识过程,由来自 20 个国家的 42 名专业人员达成共识。我们提出了一种可应用于任何 MCD 患者的诊断工作流程,以及一份全面的 MCD 相关基因列表及其相关表型。该工作流程旨在最大限度地提高诊断效果,并增加接受个性化护理以及预后和复发风险咨询的患者数量。