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硫胺素转运蛋白 2 缺乏致可逆性全面性肌张力障碍伴脑病。

Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.

机构信息

Child Neurology and Radiology Departments, Hospital Sant Joan de Déu, Barcelona, Spain.

出版信息

Mov Disord. 2012 Sep 1;27(10):1295-8. doi: 10.1002/mds.25008. Epub 2012 Jul 6.

Abstract

BACKGROUND

Thiamine transporter-2 deficiency, a condition resulting from mutations in the SLC19A3 gene, has been described in patients with subacute dystonia and striatal necrosis. The condition responds extremely well to treatment with biotin and has thus been named biotin-responsive basal ganglia disease. Recently, this deficiency has also been related to Wernicke's-like encephalopathy and atypical infantile spasms, showing heterogeneous responses to biotin and/or thiamine.

METHODS

Two Spanish siblings with a biotin-responsive basal ganglia disease phenotype and mutations in SLC19A3 presented with acute episodes of generalized dystonia, rigidity, and symmetrical lesions involving the striatum, midline nuclei of the thalami, and the cortex of cerebral hemispheres as shown by magnetic resonance imaging.

RESULTS

The clinical features resolved rapidly after thiamine administration.

CONCLUSIONS

Despite the rarity of thiamine transporter-2 deficiency, it should be suspected in patients with acute dystonia and basal ganglia injury, as thiamine can halt disease evolution and prevent further episodes. © 2012 Movement Disorder Society.

摘要

背景

硫胺素转运蛋白-2 缺乏症是由 SLC19A3 基因突变引起的一种病症,已在亚急性运动障碍和纹状体坏死患者中被描述。这种病症对生物素治疗反应极好,因此被命名为生物素反应性基底节疾病。最近,这种缺乏症也与 Wernicke 样脑病和非典型婴儿痉挛有关,对生物素和/或硫胺素的反应表现出异质性。

方法

两名患有生物素反应性基底节疾病表型和 SLC19A3 基因突变的西班牙同胞出现了全身性肌张力障碍、僵硬的急性发作,磁共振成像显示纹状体、丘脑中线核和大脑半球皮质对称性损伤。

结果

在给予硫胺素后,临床症状迅速缓解。

结论

尽管硫胺素转运蛋白-2 缺乏症较为罕见,但在出现急性肌张力障碍和基底节损伤的患者中应怀疑该病,因为硫胺素可以阻止疾病进展并预防进一步发作。© 2012 运动障碍学会。

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