Suppr超能文献

半乳糖血症与假性失神发作。

Galactosemia and phantom absence seizures.

作者信息

Aydin-Özemir Zeynep, Tektürk Pınar, Uyguner Zehra Oya, Baykan Betül

机构信息

Department of Neurology and Clinical Neurophysiology, Faculty of Medicine, Istanbul University, Istanbul, Turkey ; Department of Neurology, Memorial Ataşehir Hospital, Istanbul, Turkey.

Department of Child Neurology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

J Pediatr Neurosci. 2014 Sep-Dec;9(3):253-6. doi: 10.4103/1817-1745.147581.

Abstract

Generalized and focal seizures can rarely be seen in galactosemia patients, but absence seizures were not reported previously. An 18-year-old male was diagnosed as galactosemia at the age of 8 months. No family history of epilepsy was present. His absence seizures realized at the age of 9 years. Generalized 3-4 Hz spike-wave discharges were identified in his electroencephalography. Homozygous mutation at exon 6 c. 563A > G was identified. The electroencephalogram of his sibling was unremarkable. Our aim was to present the long-term follow-up of a patient diagnosed with galactosemia, who had phantom absence seizures and typical 3-4 Hz spike-wave discharges in his electroencephalogram to draw attention to this rare association.

摘要

全身性和局灶性癫痫发作在半乳糖血症患者中很少见,但失神发作此前未见报道。一名18岁男性在8个月大时被诊断为半乳糖血症。无癫痫家族史。他在9岁时出现失神发作。脑电图检查发现有3 - 4Hz的全身性棘慢波放电。在第6外显子发现纯合突变c. 563A > G。他兄弟姐妹的脑电图无异常。我们的目的是介绍一名被诊断为半乳糖血症患者的长期随访情况,该患者有假性失神发作且脑电图有典型的3 - 4Hz棘慢波放电,以引起对这种罕见关联的关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1049/4302547/909cac20928f/JPN-9-253-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验