| Literature DB >> 15351086 |
Masaya Kubota1, Yoichi Sakakihara, Masato Mori, Takanori Yamagata, Mariko Momoi-Yoshida.
Abstract
We here reported the clinical course and therapeutic details of a 16-year-old girl with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) who had had five stroke-like episodes (two episodes were clinically mild, while the three subsequent episodes were severe). Among the three episodes, the symptoms improved earliest and magnetic resonance spectroscopy abnormality was minimal when given L-arginine in addition to prednisolone, glycerol and edalavone. L-arginine administration during the acute phase of MELAS might be a potential therapy to reduce brain damage due to mitochondrial dysfunction.Entities:
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Year: 2004 PMID: 15351086 DOI: 10.1016/j.braindev.2004.01.006
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961