Early myoclonic encephalopathy (EME) is a rare neonatal-onset epilepsy developmental and epileptic encephalopathy (DEE) with an onset at neonatal period or during the first 3 months of life.[2] This syndrome is now included as part of the Early infantile developmental and epileptic encephalopathy (EIDEE) under the 2022 ILAE (International League Against Epilepsy) syndrome classification.[3][4]
| Early myoclonic encephalopathy[1] | |
|---|---|
| Specialty | Neurology |
Epidemiology
editThe prevalence estimates among EME are of <1 / 1 000 000.[5]
References
edit- ^ Berg, AT; Berkovic, SF; Brodie, MJ; Buchhalter, J; Cross, JH; et al. (Apr 2010). "Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009". Epilepsia. 51 (4): 676–85. doi:10.1111/j.1528-1167.2010.02522.x. PMID 20196795.676-85&rft.date=2010-04&rft_id=info:doi/10.1111/j.1528-1167.2010.02522.x&rft_id=info:pmid/20196795&rft.aulast=Berg&rft.aufirst=AT&rft.au=Berkovic, SF&rft.au=Brodie, MJ&rft.au=Buchhalter, J&rft.au=Cross, JH&rfr_id=info:sid/en.wikipedia.org:Early myoclonic encephalopathy" class="Z3988">
- ^ Guerrini, R; Aicardi, J (November 2003). "Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy)". Journal of Clinical Neurophysiology. 20 (6): 449–61. doi:10.1097/00004691-200311000-00007. PMID 14734934. S2CID 20217683.449-61&rft.date=2003-11&rft_id=https://api.semanticscholar.org/CorpusID:20217683#id-name=S2CID&rft_id=info:pmid/14734934&rft_id=info:doi/10.1097/00004691-200311000-00007&rft.aulast=Guerrini&rft.aufirst=R&rft.au=Aicardi, J&rfr_id=info:sid/en.wikipedia.org:Early myoclonic encephalopathy" class="Z3988">
- ^ Zuberi, Sameer M.; Wirrell, Elaine; Yozawitz, Elissa; Wilmshurst, Jo M.; Specchio, Nicola; Riney, Kate; Pressler, Ronit; Auvin, Stephane; Samia, Pauline; Hirsch, Edouard; Galicchio, Santiago; Triki, Chahnez; Snead, O. Carter; Wiebe, Samuel; Cross, J. Helen (June 2022). "ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions". Epilepsia. 63 (6): 1349–1397. doi:10.1111/epi.17239. ISSN 0013-9580.1349-1397&rft.date=2022-06&rft_id=info:doi/10.1111/epi.17239&rft.issn=0013-9580&rft.aulast=Zuberi&rft.aufirst=Sameer M.&rft.au=Wirrell, Elaine&rft.au=Yozawitz, Elissa&rft.au=Wilmshurst, Jo M.&rft.au=Specchio, Nicola&rft.au=Riney, Kate&rft.au=Pressler, Ronit&rft.au=Auvin, Stephane&rft.au=Samia, Pauline&rft.au=Hirsch, Edouard&rft.au=Galicchio, Santiago&rft.au=Triki, Chahnez&rft.au=Snead, O. Carter&rft.au=Wiebe, Samuel&rft.au=Cross, J. Helen&rft_id=https://onlinelibrary.wiley.com/doi/10.1111/epi.17239&rfr_id=info:sid/en.wikipedia.org:Early myoclonic encephalopathy" class="Z3988">
- ^ Djukic, A; Lado, FA; Shinnar, S; Moshé, SL (August 2006). "Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?". Epilepsy Research. 70 Suppl 1: S68-76. doi:10.1016/j.eplepsyres.2005.11.022. PMID 16829044. S2CID 22914424.
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Early myoclonic encephalopathy". www.orpha.net.
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