Successful management of refractory epilepsy in creatine transporter deficiency with cannabidiol and clobazam: A case report

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-12-16 DOI:10.1002/epi4.13116
Maria Borrell-Pichot, Carmen Fons, Susana Boronat, Alba Sierra-Marcos
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Abstract

Creatine transporter deficiency (CRTR-D) is a rare X-linked inherited disease belonging to the group of cerebral creatine deficiency disorders. Major clinical features include developmental delay and epilepsy. To date, fewer than 200 individuals with CRTR-D have been reported. As a result, there is little evidence for effective treatment. Available therapies are creatine precursors, with a mild effect on disease progression. Concerning epilepsy, standard management is recommended and no specific anti-seizure medication (ASM) has been shown to be effective in refractory cases. We report the case of a 28-year-old male patient with CRTR-D and childhood-onset refractory epilepsy. He had an average of 10–20 focal motor seizures with impaired consciousness per month. He had tried several ASMs without significant improvement. Treatment with cannabidiol (CBD) and clobazam (CLB) in combination was added. The patient became seizure-free from the first week, and up to 1 year of follow-up. Behavioral improvement was also noted by his caregivers. No adverse effects were reported. Very few cases of CRTR-D with refractory epilepsy have been reported. This calls for more extensive research and suggests a possible role for CBD in cerebral creatine metabolism and transport and valuable option for future studies.

Plain Language Summary

Creatine transporter deficiency (CRTR-D) is a rare genetic disorder causing mental, behavioral, and movement problems. More than half of patients also have seizures, but because there are fewer than 200 known cases, it is difficult to know the best treatment options. We present a 28-year-old man with CRTR-D who had severe developmental delays and frequent seizures since childhood, despite trying many medications. After starting cannabidiol and clobazam, he has been seizure-free for a year. Sharing this success might help other people with CRTR-D benefit from similar treatments.

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用大麻二酚和氯巴赞成功治疗肌酸转运体缺乏症难治性癫痫:病例报告。
肌酸转运蛋白缺乏症(CRTR-D)是一种罕见的x连锁遗传性疾病,属于脑肌酸缺乏症。主要临床特征包括发育迟缓和癫痫。迄今为止,报道的CRTR-D患者不到200人。因此,几乎没有有效治疗的证据。可用的治疗方法是肌酸前体,对疾病进展有轻微影响。对于癫痫,建议采用标准管理,目前尚无特异性抗癫痫药物(ASM)对难治性病例有效。我们报告一例28岁的男性患者与CRTR-D和儿童期起病难治性癫痫。他平均每个月有10-20次局灶性运动发作伴有意识受损。他尝试了几次asm,但没有明显改善。加入大麻二酚(CBD)和氯巴唑(CLB)联合治疗。患者从第一周开始无癫痫发作,随访长达1年。照顾他的人也注意到他的行为有所改善。无不良反应报告。CRTR-D合并难治性癫痫的病例报道很少。这需要更广泛的研究,并提出CBD在脑肌酸代谢和运输中的可能作用,为未来的研究提供了有价值的选择。摘要:肌酸转运蛋白缺乏症(CRTR-D)是一种罕见的遗传性疾病,可引起精神、行为和运动问题。超过一半的患者也有癫痫发作,但由于已知病例不到200例,因此很难知道最佳治疗方案。我们报告一位患有CRTR-D的28岁男性患者,尽管尝试了许多药物治疗,但他自童年起就有严重的发育迟缓和频繁的癫痫发作。在服用大麻二酚和氯巴唑后,他已经一年没有癫痫发作了。分享这一成功可能会帮助其他CRTR-D患者从类似的治疗中受益。
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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
期刊最新文献
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