Article
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia - 1 Feb 2020
Gasser Marius, Boonsimma Ponghatai, Netbaramee Wiracha, Wechapinan Thanin, Srichomthomg Chalurmpon, Ittiwut Chupong, Krenn Martin, Zimprich Fritz, Milenkovic Ivan, Abicht Angela, Biskup Saskia, Roser Timo, Shotelersuk Vorasuk, Tacke Moritz, Kuersten Marianne, Wagner Matias, Borggraefe Ingo, Suphapeetiporn Kanya, von Stülpnagel Celina
Abstract excerpt
ATP1A3 related disease is a clinically heterogeneous condition currently classified as alternating hemiplegia of childhood, rapid-onset dystonia-parkinsonism and cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss. Recently, it has become apparent that a remarkably large subgroup is suffering from often difficult-to-treat epilepsy. The aim of the present study was to assess the...
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