儿童MOGAD痫性发作的诊疗发展
Advances in Diagnosis and Treatment of Seizures in Pediatric MOGAD
DOI: 10.12677/acm.2026.1651863, PDF,   
作者: 彭怡洁, 李秀娟*:重庆市重庆医科大学附属儿童医院神经内科,儿童少年健康与疾病国家临床医学研究中心,儿童发育疾病研究教育部重点实验室,儿童神经发育与认知障碍重庆市重点实验室,重庆
关键词: 髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)痫性发作临床特点治疗儿童Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD) Seizures Clinical Features Treatment Children
摘要: 髓鞘少突胶质细胞糖蛋白抗体相关疾病(myelin oligodendrocyte glycoprotein antibody associated disease, MOGAD)是由MOG抗体介导的中枢神经系统炎性脱髓鞘疾病,在儿童中具有独特的临床特征。痫性发作是儿童MOGAD常见的临床表现之一,发生率高达20%~40%,远高于其他炎性脱髓鞘疾病。既往有关MOGAD痫性发作研究多集中成人群体,儿童群体研究较为有限。故本文旨在系统综述儿童群体MOGAD痫性发作的诊疗发展,并且从病理机制、临床特征及治疗策略这几个方面开展详细描述,为临床早期诊断和精确诊疗提供科学参考依据。
Abstract: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory demyelinating disease of the central nervous system mediated by MOG antibodies, with a relatively high incidence among children. Seizures are one of the common clinical manifestations of MOGAD in children, with an incidence as high as 20%~40%, which is significantly higher than that of other inflammatory demyelinating diseases. Previous studies on MOGAD seizures have primarily focused on adult populations, while research on pediatric populations remains limited. Therefore, this article aims to provide a systematic review of the diagnostic and therapeutic developments regarding MOGAD-associated seizures in children. It offers a detailed description of the pathological mechanisms, clinical features, and treatment strategies to provide a scientific basis for early clinical diagnosis and precise management.
文章引用:彭怡洁, 李秀娟. 儿童MOGAD痫性发作的诊疗发展[J]. 临床医学进展, 2026, 16(5): 695-701. https://doi.org/10.12677/acm.2026.1651863

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