Adult-onset status epilepticus in patients with COQ8A coenzyme Q10 deficiency: A case series

IF 1.8 Q3 CLINICAL NEUROLOGY
Panagiota-Eleni Tsalouchidou , Clara Juenemann , Wiebke Hahn , Felix Zahnert , Leona Möller , Lukas Hakel , André Kemmling , Katja Menzler , Ole J. Simon , Lars Timmermann , Susanne Knake , Felix Bernhard
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Abstract

This case series describes the clinical features, diagnostic challenges, treatment approaches, and outcomes of three adult patients with COQ8A-related CoQ10 deficiency presenting with focal status epilepticus, who were effectively treated at the Department of Neurology, Philipps University Marburg, Marburg, Germany. The patients, all from consanguineous families with the first two being siblings, presented with a late onset of the disease, characterized by progressive cerebellar ataxia and epilepsy, with clinical deterioration and focal status epilepticus occurring in adulthood. The first patient exhibited myoclonic status, while the second and third patients presented with bilateral tonic-clonic seizures followed by focal status epilepticus manifesting with cortical blindness. Despite differing semiologies, all patients displayed similar EEG findings with continuous or nearly continuous occipital sharp waves and spikes. MRI findings revealed focal changes in the Diffusion-Weighted Imaging (DWI) and Fluid Attenuated Inversion Recovery (FLAIR) sequences. Significant clinical improvement was observed following treatment with high doses of CoQ10, with the diffusion restriction abnormalities being reversible after therapy. In conclusion, consistent with existing literature, we observed a characteristic EEG pattern that can help identify the disease and facilitate early diagnosis and treatment. The diffusion restriction abnormalities on MRI were reversible after therapy, and high doses of CoQ10 proved beneficial even in cases of status epilepticus.
COQ8A 辅酶 Q10 缺乏症患者的成人癫痫状态:病例系列
本系列病例描述了三名患有 COQ8A 相关 CoQ10 缺乏症并伴有局灶性癫痫的成年患者的临床特征、诊断难题、治疗方法和疗效,德国马尔堡菲利普斯大学神经病学系对这些患者进行了有效治疗。这些患者均来自近亲结婚家庭,前两名患者是同胞兄弟姐妹,起病较晚,以进行性小脑共济失调和癫痫为特征,成年后出现临床恶化和局灶性癫痫状态。第一名患者表现为肌阵挛性状态,第二名和第三名患者表现为双侧强直-阵挛发作,随后出现局灶性癫痫状态,表现为皮层失明。尽管半身状态不同,但所有患者的脑电图表现相似,均为连续或几乎连续的枕叶尖波和棘波。核磁共振成像(MRI)结果显示,弥散加权成像(DWI)和流体衰减反转恢复(FLAIR)序列出现局灶性改变。使用大剂量辅酶Q10治疗后,临床症状明显改善,弥散限制异常在治疗后可逆转。总之,与现有文献一致,我们观察到了一种特征性的脑电图模式,这种模式有助于鉴别该疾病并促进早期诊断和治疗。核磁共振成像上的弥散受限异常在治疗后是可逆的,大剂量辅酶Q10甚至对癫痫状态病例也有益处。
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来源期刊
Epilepsy and Behavior Reports
Epilepsy and Behavior Reports Medicine-Neurology (clinical)
CiteScore
2.70
自引率
13.30%
发文量
54
审稿时长
50 days
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