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EnglishBenign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.
| Autori: | |
| Titolo: | Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family. |
| Data di pubblicazione: | 2003 |
| Abstract: | Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder. |
| Lingua: | Inglese |
| Rivista: | |
| Citazione: | Vaccario, M. L., Valenti, M. A., Carullo, A., Di Bartolomeo, R., Mazza, S., Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family., <<CLINICAL ELECTROENCEPHALOGRAPHY>>, 2003; 34 (Gennaio): 15-17 [http://hdl.handle.net/10807/11312] |
| Appare nelle tipologie: | Articolo in rivista, Nota a sentenza |
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