LoVoi Jonathan, Thai Don Q, Han Jennifer, Wang Sophia, Agonafer Makeda, Thankappan Baburaj
From the Neuroscience Institute, UW Medicine - Valley Medical Center, Renton, WA.
Neurol Genet. 2024 Sep 18;10(5):e200184. doi: 10.1212/NXG.0000000000200184. eCollection 2024 Oct.
Describe a case of stroke-like episodes and refractory status epilepticus diagnosed with primary CoQ10 deficiency-4 (COQ10D4) using whole-exome sequencing in the intensive care unit (ICU), with treatment implications.
A patient presented to the emergency department with 1 month of progressively worsening focal motor status epilepticus and stroke-like imaging abnormalities. Multiple seizure medications, ketogenic diet, and elective intubation for anesthetic drips failed to achieve sustained seizure freedom. Genetic testing was pursued for prognostic information and identified potential treatment.
Whole-exome sequencing revealed compound heterozygous variants of , including 1 allele not previously described as pathogenic. The patient's history, imaging, and genetic testing supported a diagnosis of COQ10D4. High-dose coenzyme Q10 supplementation was started with gradual clinical improvement.
Whole-exome sequencing is a fast and cost-effective means to diagnose rare neurologic disease in critically ill patients and can uncover treatment options. While primarily used in the neonatal ICU, appropriately selected adult patients may also benefit.
描述一例在重症监护病房(ICU)通过全外显子组测序诊断为原发性辅酶Q10缺乏症4型(COQ10D4)的类中风发作和难治性癫痫持续状态病例,并探讨其治疗意义。
一名患者因进行性加重的局灶性运动性癫痫持续状态和类中风影像学异常1个月就诊于急诊科。多种抗癫痫药物、生酮饮食以及为使用麻醉剂进行的择期插管均未能实现癫痫持续缓解。进行基因检测以获取预后信息并确定潜在治疗方法。
全外显子组测序发现了复合杂合变异,包括1个以前未被描述为致病性的等位基因。患者的病史、影像学检查和基因检测支持COQ10D4的诊断。开始补充高剂量辅酶Q10后,临床症状逐渐改善。
全外显子组测序是诊断重症患者罕见神经系统疾病的一种快速且经济有效的方法,并且可以发现治疗选择。虽然主要用于新生儿ICU,但适当选择的成年患者也可能受益。