Lin Jaime, Chiconelli Faria Eliete, Da Rocha Antônio José, Rodrigues Masruha Marcelo, Pereira Vilanova Luiz Celso, Scheper Gert C, Van der Knaap Marjo S
Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil.
J Child Neurol. 2010 Nov;25(11):1425-8. doi: 10.1177/0883073810370897. Epub 2010 May 25.
Leukoencephalopathy with brainstem and spinal cord involvement and elevated brain lactate diagnosis is based on its highly characteristic pattern of abnormalities observed by magnetic resonance imaging and spectroscopy. Clinically, affected patients develop slowly progressive cerebellar ataxia, spasticity, and dorsal column dysfunction, sometimes with a mild cognitive deficit or decline. In 2007, the pathophysiology of this disorder was elucidated with the discovery of mutations in the DARS2 gene, which encodes mitochondrial aspartyl-tRNA synthetase, in affected individuals. Here, the authors present a case of leukoencephalopathy with brainstem and spinal cord involvement with normal brain lactate, in which genetic analysis revealed a new mutation in the DARS2 gene not previously described.
伴有脑干和脊髓受累及脑乳酸升高的白质脑病的诊断基于磁共振成像和波谱观察到的高度特征性异常模式。临床上,受影响的患者会出现缓慢进展的小脑共济失调、痉挛和后索功能障碍,有时伴有轻度认知缺陷或衰退。2007年,随着在受影响个体中发现编码线粒体天冬氨酰 - tRNA合成酶的DARS2基因突变,阐明了这种疾病的病理生理学。在此,作者报告一例伴有脑干和脊髓受累但脑乳酸正常的白质脑病病例,其中基因分析揭示了一个此前未描述的DARS2基因新突变。