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Publicaciones científicas

Musicogenic seizures in Dravet syndrome

20-mar-2013 | Revista: Developmental Medicine and Child Neurology

Sanchez-Carpintero R, Patiño-Garcia A, Urrestarazu E.
Paediatric Neurology Unit, Clínica Universidad de Navarra, Pamplona


RESUMEN

Dravet syndrome is an epileptic encephalopathy characterized by multiple types of seizures. We report the first case of musicogenic reflex seizures in a 7-year-old male with a mutation in the SCN1A gene causing Dravet syndrome. Reflex seizures have been reported in patients with Dravet syndrome provoked by body temperature elevation, looking at visual patterns, or under intermittent photic stimulation. The case we report widens the spectrum of reflex seizures recorded in patients with Dravet syndrome. Cortical hyperexcitability of genetic origin could explain the tendency of these patients to experience reflex seizures.

CITA DEL ARTÍCULO   2013 Mar 20. doi: 10.1111/dmcn.12138