Resumo

ESCALANTE-GAVANCHO, Carlos et al. MELAS in Peru: case report. Rev Neuropsiquiatr [online]. 2015, vol.78, n.4, pp.253-257. ISSN 0034-8597.

MELAS syndrome is a rare mitochondrial cytopathy difficult to diagnose. We report the case of a 10year old girl who was admitted to the National Institute of Neurological Sciences of Lima - Peru, who presented sudden stroke like episodes and seizures. Neuroimaging studies showed infarction and genetic testing was positive for identifying the most common MELAS mutation(A3243).

Palavras-chave : Infarction; mutation A3243G; lactic acidosis; mitochondrial myopathy.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )