Literature DB >> 24225564

[A case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) with treatment-resistant status epilepticus that was effectively treated with lamotrigine].

Toru Kai1, Shuichiro Masuda, Hiroyasu Tokunaga, Shigeaki Hayashi, Tatsui Nagado, Yoshikazu Maruyama.   

Abstract

A 16-year-old woman with MELAS developed fever and myoclonic epilepsy which improved with conventional anti-epileptic drugs. Since seizures recurred one month after successful treatment, the doses of phenobarbital, clonazepan, and valproate were increased. However, there was no improvement and status epilepticus continued. The addition of lamotrigine resulted in a decreased frequency and good control of seizures. This case is important, showing satisfactory results from the addition of lamotrigine for treatment-resistant status epilepticus.

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Year:  2013        PMID: 24225564     DOI: 10.5692/clinicalneurol.53.809

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  2 in total

1.  Association between stroke-like episodes and neuronal hyperexcitability in MELAS with m.3243A>G: A case report.

Authors:  Shota Sakai; Masato Osaki; Masaoki Hidaka; Shunsuke Kimura; Yuichiro Ohya; Tetsuro Ago; Takanari Kitazono; Shuji Arakawa
Journal:  eNeurologicalSci       Date:  2018-08-22

2.  Rare Phenotypic Manifestations of MELAS.

Authors:  Josef Finsterer
Journal:  Yonsei Med J       Date:  2020-10       Impact factor: 2.759

  2 in total

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