Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia

被引:43
|
作者
Capovilla, Giuseppe [1 ]
Striano, Pasquale [2 ]
Gambardella, Antonio [4 ]
Beccaria, Francesca [1 ]
Hirsch, Edouard [5 ]
Casellato, Susanna [6 ]
Romeo, Antonino [7 ]
Rubboli, Guido [8 ]
Sofia, Vito [9 ]
Teutonico, Federica [10 ]
Valenti, Maria Paola [5 ]
Striano, Salvatore [3 ]
机构
[1] Osped C Poma, Dept Child Neuropsychiat, I-6100 Mantova, Italy
[2] Inst G Gaslini, Muscular & Neurodegenerat Dis Unit, Genoa, Italy
[3] Univ Naples Federico 2, Epilepsy Ctr, Naples, Italy
[4] Magna Graecia Univ Catanzaro, Sch Med, Inst Neurol, Catanzaro, Italy
[5] Strasbourg Univ, Epilepsy Ctr, Dept Neurol, Strasbourg, France
[6] Univ Sassari, Dept Child Neuropsychiat, I-07100 Sassari, Italy
[7] AO Fatebenefratelli & Oftalm, Ctr Child Epilepsy, Milan, Italy
[8] Univ Bologna, Bellaria Hosp, Dept Neurosci, Div Neurol, Bologna, Italy
[9] Univ Catania, Dept Neurosci, Epilepsy Ctr, Catania, Italy
[10] C Mondino Inst, Dept Child Neuropsychiat, Pavia, Italy
关键词
EMA; Eyelid myoclonic epilepsy; Intellectual impairment; Mental retardation; Generalized epilepsy; NONCONVULSIVE STATUS EPILEPTICUS; MENTAL-RETARDATION; FIXATION-OFF; VIDEO-EEG; ABSENCES; CLOSURE; SENSITIVITY; ADULT;
D O I
10.1111/j.1528-1167.2008.02002.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: This retrospective study aims to review the electroclinical features of patients presenting with eyelid myoclonia (EM) with and without absences. Methods: The Italian chapter of the International League Against Epilepsy (ILAE) has been conducting an electroclinical study of patients with EM. Among these, we searched for and selected the patients presenting with both impairment of intellectual functions and a peculiar ictal electroencephalography (EEG) pattern, that is, a discharge of fast generalized polyspikes/polyspikes and waves. Results: We found 18 patients matching this electroclinical picture. All the patients were photosensitive. All of them had associated generalized, mostly nocturnal, tonic-clonic seizures. During the evolution, 13 patients presented episodes of EM status. Despite adequate antiepileptic treatment, the patients remained drug resistant for many years or throughout the evolution. The degree of impairment of intellectual functions varied from borderline level to moderate mental retardation. Discussion: The patients we described herein can be considered a homogeneous group in the more heterogeneous group of patients presenting with EM. Further clinical and, more probably, genetic studies will clarify whether this condition could be considered a specific and homogeneous condition in the more heterogeneous group of patients presenting with EM.
引用
收藏
页码:1536 / 1541
页数:6
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