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两例携带EARS2基因新突变导致的伴有丘脑和脑干受累及高乳酸血症的白质脑病的同胞病例

Leukoencephalopathy with thalamus and brainstem involvement and high lactate caused by novel mutations in the EARS2 gene in two siblings.

作者信息

Şahin Sevim, Cansu Ali, Kalay Ersan, Dinçer Tuba, Kul Sibel, Çakır İsmet Miraç, Kamaşak Tülay, Budak Gülden Yorgancıoğlu

机构信息

Department of Pediatric Neurology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey.

Department of Pediatric Neurology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey.

出版信息

J Neurol Sci. 2016 Jun 15;365:54-8. doi: 10.1016/j.jns.2016.04.008. Epub 2016 Apr 9.

Abstract

Leukoencephalopathy with thalamus and brainstem involvement, and high lactate (LTBL) is a recently identified disease related to mutations in the EARS2 gene encoding glutamyl-tRNA synthetase. We report clinical and radiological findings for two siblings with new pathogenic mutations in the EARS2 gene. Both patients showed symptoms of mild-type disease, but there were clinical differences between the two siblings. While the older brother had hypotonia and delayed developmental milestones, the younger brother had seizures and spasticity in the lower extremities. Brain magnetic resonance imaging (MRI) findings were quite similar for the two siblings. MRI findings were specific to LTBL. MRI lesions of the older sibling had regressed over time. Clinical and radiological improvement, as in the previously reported patients with LTBL, may be an important clue for diagnosis.

摘要

伴有丘脑和脑干受累及高乳酸血症的白质脑病(LTBL)是一种最近发现的与编码谷氨酰胺 - tRNA合成酶的EARS2基因突变相关的疾病。我们报告了两名患有EARS2基因新致病突变的兄弟姐妹的临床和影像学表现。两名患者均表现出轻型疾病的症状,但两兄弟之间存在临床差异。哥哥有肌张力减退和发育里程碑延迟,而弟弟有癫痫发作和下肢痉挛。两名兄弟姐妹的脑磁共振成像(MRI)表现非常相似。MRI表现是LTBL所特有的。哥哥的MRI病变随时间推移有所消退。正如之前报道的LTBL患者一样,临床和影像学改善可能是诊断的重要线索。

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