Abstract
Neuronal migration disorders are rare malformations which can be associated with epileptic seizures. We report about a 14-year-old female patient suffering from epilepsy with infantile spasms, myoclonic-astatic seizures and absences. The EEG showed generalized 2.5-3/sec spike-wave paroxysms. As the possible cause of the disease the MRI scan exhibited a bilateral band heterotopia.
MeSH terms
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Adolescent
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Age of Onset
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Brain / diagnostic imaging
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Brain / physiopathology
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Brain Diseases / complications
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Brain Diseases / diagnostic imaging
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Brain Diseases / physiopathology
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Cell Movement
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Electroencephalography
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Epilepsy, Generalized / complications
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Epilepsy, Generalized / diagnosis
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Epilepsy, Generalized / physiopathology*
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Female
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Humans
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Infant
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Magnetic Resonance Imaging
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Neurons
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Radiography
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Spasms, Infantile / complications
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Spasms, Infantile / diagnosis
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Spasms, Infantile / physiopathology