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意外摄入乙醇后发生生物素-硫胺素反应性基底节疾病:一例报告

Developing of Biotin-Thiamine Responsive Basal Ganglia Disease after Accidental Ingestion of Ethyl Alcohol: A Case Report.

作者信息

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

机构信息

Department of Pediatrics, King Fahad Hospital, AlBaha, Saudi Arabia.

Al Taif Children Hospital, Taif, Saudi Arabia.

出版信息

J Epilepsy Res. 2023 Dec 31;13(2):59-62. doi: 10.14581/jer.23010. eCollection 2023 Dec.

Abstract

Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare, inherited neurometabolic disorder caused by mutations in the 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 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.

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障碍,由该基因的突变引起,其特征为复发性亚急性脑病发作,常由感染引发。BTBGD患者具有典型的神经影像学表现,对高剂量硫胺素反应显著。在此,我们报告一名2岁半的沙特女孩,急性起病,出现共济失调、言语不清和吞咽困难,1天前有意外摄入约20毫升用于调配香水的乙醇的病史。她的哥哥有类似的临床表现,被诊断为BTBGD。该患者神志完全清醒,能完整地说出句子,但存在构音障碍。她无法独立行走。检查显示乙醇毒性检测呈阳性(10毫克/分升),脑部磁共振成像显示基底节改变与BTBGD相符。对高剂量硫胺素的显著反应提示该基因是一个强有力的候选基因,桑格测序显示纯合突变(NM_025243.4):c.1264A>G(p.Thr422Ala)。BTBGD患者应谨慎并注意乙醇产品,其可能导致BTBGD危机。对推荐剂量无反应的患者可能需要给予高剂量硫胺素。需要进一步的临床研究来确定最佳剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f31e/10783965/b8ea89c078fe/jer-23010f1.jpg

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Biotin-Thiamine-Responsive Basal Ganglia Disease in Children: A Treatable Neurometabolic Disorder.
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3
Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening.
Ann Clin Transl Neurol. 2019 Oct;6(10):2097-2103. doi: 10.1002/acn3.50898. Epub 2019 Sep 26.
4
Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies.
J Inherit Metab Dis. 2019 Jul;42(4):581-597. doi: 10.1002/jimd.12125. Epub 2019 Jun 24.
5
Psychological Assessment of Patients With Biotin-Thiamine-Responsive Basal Ganglia Disease.
Child Neurol Open. 2017 Sep 14;4:2329048X17730742. doi: 10.1177/2329048X17730742. eCollection 2017 Jan-Dec.
7
Free-thiamine is a potential biomarker of thiamine transporter-2 deficiency: a treatable cause of Leigh syndrome.
Brain. 2016 Jan;139(Pt 1):31-8. doi: 10.1093/brain/awv342. Epub 2015 Dec 10.
8
Defects of thiamine transport and metabolism.
J Inherit Metab Dis. 2014 Jul;37(4):577-85. doi: 10.1007/s10545-014-9712-9. Epub 2014 May 1.
9
Thiamine deficiency in critically ill patients with sepsis.
J Crit Care. 2010 Dec;25(4):576-81. doi: 10.1016/j.jcrc.2010.03.003. Epub 2010 Jun 19.
10
Mutations in a thiamine-transporter gene and Wernicke's-like encephalopathy.
N Engl J Med. 2009 Apr 23;360(17):1792-4. doi: 10.1056/NEJMc0809100.

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