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重新评估库伦-德弗里斯综合征中的脑电图监测:一例局灶性意识障碍性癫痫延迟诊断病例

Reevaluating Electroencephalography Monitoring in Koolen-de Vries Syndrome: A Case of Delayed Focal Impaired Consciousness Seizure Diagnosis.

作者信息

Nazari Ryan, Nayeni Manav, Sakhamuru Pavan, Gupta Anuj, Moylan Charles V

机构信息

College of Osteopathic Medicine, Kansas City University, Kansas City, USA.

Department of Pediatrics, Pediatric Associates - Children's Mercy Health Network, Kansas City, USA.

出版信息

Cureus. 2025 May 7;17(5):e83693. doi: 10.7759/cureus.83693. eCollection 2025 May.

Abstract

Koolen-de Vries syndrome (KdVS) is a rare multisystem genetic disorder due to deletions in the KANSL1 gene. The most common type of seizure documented in these patients is focal impaired consciousness seizure (FICS). These seizures present with difficult-to-distinguish characteristics, including autonomic symptoms, brief loss of consciousness, and post-ictal confusion. The ambiguity of this presentation can make it difficult to detect clinically. This case presents an eight-year-old male child with KdVS who presented to the clinic with complaints of increased outbursts, spatial disorientation, issues with mood and self-regulation, and episodes of "spacing out" as noted by his teacher. The initial diagnosis was dysautonomia and was conservatively managed. However, due to worsening neurocognitive outcomes, neurological referral and work-up were initiated to further elucidate the etiology of his symptoms. The patient's electroencephalography (EEG) findings showed frequent focal sharp waves consistent with FICS. He was then treated accordingly with diazepam and amantadine, which led to a significant improvement in neurological status. This case highlights the importance of the use of EEG in KdVS patients, as well as the implications of implementing guidelines recommending the low threshold required for use of EEG and full neurological work-up for patients with any alarm symptoms possibly indicative of FICS or other epileptiform activity.

摘要

库伦-德弗里斯综合征(KdVS)是一种罕见的多系统遗传性疾病,由KANSL1基因缺失引起。这些患者中记录到的最常见癫痫发作类型是局灶性意识障碍发作(FICS)。这些发作具有难以区分的特征,包括自主神经症状、短暂意识丧失和发作后意识模糊。这种表现的模糊性可能使其在临床上难以检测。本病例介绍了一名患有KdVS的8岁男童,他因爆发性增加、空间定向障碍、情绪和自我调节问题以及老师提到的“发呆”发作而就诊。初步诊断为自主神经功能障碍,并进行了保守治疗。然而,由于神经认知结果恶化,启动了神经科转诊和检查,以进一步阐明其症状的病因。患者的脑电图(EEG)结果显示频繁的局灶性尖波,与FICS一致。然后相应地用安定和金刚烷胺对他进行治疗,这导致神经状态有显著改善。本病例强调了在KdVS患者中使用脑电图的重要性,以及实施指南的意义,该指南建议对任何可能提示FICS或其他癫痫样活动的警报症状患者,使用脑电图和全面神经检查的阈值要低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/12144403/1407950ab914/cureus-0017-00000083693-i01.jpg

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