Eyelid myoclonia with absences (Jeavons syndrome): A well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?

被引:101
作者
Striano, Salvatore [1 ]
Capovilla, Giuseppe [2 ]
Sofia, Vito [3 ]
Romeo, Antonino [4 ]
Rubboli, Guido [5 ]
Striano, Pasquale [6 ]
Trenite, Dorothee Kasteleijn-Nolst [7 ]
机构
[1] Univ Naples Federico II, Epilepsy Ctr, Dept Neurol Sci, I-80131 Naples, Italy
[2] C Poma Hosp, Dept Child Neuropsychiat, Mantua, Italy
[3] Univ Catania, Dept Neurosci, Epilepsy Ctr, Catania, Italy
[4] Fatebenefratelli Hosp, Milan, Italy
[5] Bellaria Hosp, Dept Neurosci, Bologna, Italy
[6] Inst G Gaslini, Muscular & Neurodegenerat Dis Unit, Genoa, Italy
[7] Univ Roma La Sapienza, Fac Med 2, Dept Neurol, Rome, Italy
关键词
Eyelid myoclonia; Eyelid myoclonia with absences; Epilepsy; Myoclonus; Photosensitivity;
D O I
10.1111/j.1528-1167.2009.02114.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Eyelid myoclonia with absences (EMA), or Jeavons syndrome, is a generalized epileptic condition clinically characterized by eyelid myoclonia (EM) with or without absences, eye closure-induced electroencephalography (EEG) paroxysms, and photosensitivity; in addition, rare tonic-clonic seizures may also occur. Although first described in 1977 and widely reported by several authors within the last few years, EMA has not been yet recognized as a definite epileptic syndrome. However, when strict criteria are applied to the diagnosis, EMA appears to be a distinctive condition that could be considered a myoclonic epileptic syndrome, with myoclonia limited to the eyelids, rather than an epileptic syndrome with absences.
引用
收藏
页码:15 / 19
页数:5
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