意外摄入乙醇后出现生物素-硫胺素反应性基底节疾病:病例报告

Abdullah Nasser Aldosari, Aida Arisha, Ahmed Ibrahim, Mohamed Gongi
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摘要

生物素-硫胺素反应性基底节疾病(BTBGD)是一种罕见的遗传性神经代谢疾病,由 SLC19A3 基因突变引起,其特征是反复发作的亚急性脑病,通常由感染引发。BTBGD患者有典型的神经影像学表现,对大剂量硫胺素反应剧烈。在此,我们报告了一名两岁半的沙特女孩,她因共济失调、言语不清和吞咽困难急性发病,发病前一天曾意外摄入约 20 毫升用于配制香水的乙醇。她的哥哥也有类似的临床表现,被诊断为 BTBGD。患者完全清醒,能说完整的句子,但有构音障碍。她无法独立行走。调查显示,乙醇毒性测试呈阳性(10 毫克/分升),脑磁共振成像显示基底节变化与 BTBGD 一致。对大剂量硫胺素的剧烈反应表明 SLC19A3 是一个强有力的候选基因,桑格测序发现了一个同源基因(NM_025243.4):c.1264A>G (p.Thr422Ala) 突变。BTBGD 患者应谨慎使用乙醇产品,因为乙醇产品可能导致 BTBGD 危象。对推荐剂量无效的患者可能需要服用大剂量硫胺素。确定最佳剂量还需要进一步的临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developing of Biotin-Thiamine Responsive Basal Ganglia Disease after Accidental Ingestion of Ethyl Alcohol: A Case Report
Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare, inherited neurometabolic disorder caused by mutations in the SLC19A3 gene and characterized by recurrent sub-acute episodes of encephalopathy that are often triggered by infections. Patients with BTBGD have classical neuroimaging findings and a dramatic response to high doses of thiamine. Herein, we report a 2 and a half-year-old Saudi girl presented with an acute onset of ataxia, slurred speech, and dysphagia, which was preceded by a history of accidental ingestion of around 20 mL of ethyl alcohol that is used in formulating perfumes 1 day earlier. Her older brother had a similar clinical presentation and was diagnosed with BTBGD. The patient was fully alert and spoke in full sentences with dysarthria. She was unable to walk unassisted. Investigation revealed a positive toxicity test for ethyl alcohol (10 mg/dL), and brain magnetic resonance imaging showed basal ganglia changes consistent with BTBGD. The dramatic response to high doses of thiamine suggested SLC19A3 as a strong candidate gene, and Sanger sequencing revealed a homozygous (NM_025243.4): c.1264A>G (p.Thr422Ala) mutation. Patients with BTBGD should be cautious and aware of ethyl alcohol products, which can lead to a BTBGD crisis. The administration of a high dose of thiamin may be required in patients who have not responded to the recommended dose. Further clinical research is required to determine the optimal doses.
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