Short-latency somatosensory evoked potentials in dystrophia myotonica.
AUTOR(ES)
Bartel, P R
RESUMO
Somatosensory evoked potentials (SEPs) were recorded in a group of 21 patients with dystrophia myotonica and in a group of controls. Those with dystrophia myotonica had longer absolute peak latencies due to slower peripheral conduction. SEP abnormalities revealed peripheral and/or central conduction delays in 33% of the dystrophia myotonica subjects. There was no apparent relationship between the clinical severity of the disease and SEP abnormality.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1027831Documentos Relacionados
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