Benign infantile seizures (a French collaborative study).

被引:9
作者
Gautier, A
Pouplard, E
Bednarek, N
Motte, J
Berquin, P
Billard, C
Boidein, F
Boulloche, J
Dulac, O
Échenne, B
Humbertclaude, V
机构
[1] CHU Angers, Ctr Robert Debre, Dept Pediat Med, Unite Neuropediat, F-49033 Angers 01, France
[2] Amer Mem Hosp, F-51092 Reims, France
[3] Hop Nord, F-80054 Amiens, France
[4] Hop Clocheville, F-37042 Tours, France
[5] Ctr Hosp St Antoine, F-59019 Lille, France
[6] Hop Flaubert, Serv Neurol Pediat, F-76033 Le Havre, France
[7] Hop St Vincent de Paul, Serv Neuropediat, F-75014 Paris, France
[8] Clin St Eloi, F-34059 Montpellier, France
来源
ARCHIVES DE PEDIATRIE | 1999年 / 6卷 / 01期
关键词
seizures; infant;
D O I
10.1016/S0929-693X(99)80070-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. - Benign infantile non febrile seizures are not well known, leading us to study their clinical and EEG characteristics. Methods. - Between 1981 and 1994, we assembled 34 patients with the following inclusion criteria; non febrile seizures between 1 month and 2 years of age, normal personal history, no abnormality on clinical, biological and radiological investigations, normal developmental outcome with a least 1 year follow-up. Results. - These 34 patients were recognized as 14 familial cases (identical seizures affecting parents) and 11 non familial cases. The other nine cases had different or undefined epilepsy in the family. The clinical and EEG characteristics were the same; at the mean age of 6 months, brief partial seizures (often secondarily or apparently generalized) occurring in a cluster of two to 12 episodes a day for mean duration of 2.5 days with ictal EEG showing focal discharge, often slow waves or focal spikes on post-ictal tracing and normal interictal EEG. Conclusion. - The clinical and EEG characteristics are important in order to recognize this type of infantile convulsions (familial or not familial), which have a good prognosis and need no aggressive treatment. (C) 1999 Elsevier, Paris.
引用
收藏
页码:32 / 39
页数:8
相关论文
共 8 条
[1]   Benign familial infantile convulsions. [J].
Échenne, B ;
Rivier, F ;
Humbertclaude, V ;
Roubertie, A ;
Cheminal, R ;
Malafosse, A .
ARCHIVES DE PEDIATRIE, 1999, 6 (01) :54-58
[2]  
FUKUYAMA Y, 1963, CLIN PSYCHIATR, V5, P211
[3]   BENIGN FAMILIAL INFANTILE EPILEPSY [J].
LEE, WL ;
LOW, PS ;
RAJAN, U .
JOURNAL OF PEDIATRICS, 1993, 123 (04) :588-590
[4]   Familial infantile convulsions and paroxysmal choreoathetosis: A new neurological syndrome linked to the pericentromeric region of human chromosome 16 [J].
Szepetowski, P ;
Rochette, J ;
Berquin, P ;
Piussan, C ;
Lathrop, GM ;
Monaco, AP .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) :889-898
[5]   BENIGN INFANTILE FAMILIAL CONVULSIONS [J].
VIGEVANO, F ;
FUSCO, L ;
DICAPUA, M ;
RICCI, S ;
SEBASTIANELLI, R ;
LUCCHINI, P .
EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (08) :608-612
[6]   BENIGN COMPLEX PARTIAL EPILEPSIES IN INFANCY [J].
WATANABE, K ;
YAMAMOTO, N ;
NEGORO, T ;
TAKAESU, E ;
ASO, K ;
FURUNE, S ;
TAKAHASHI, I .
PEDIATRIC NEUROLOGY, 1987, 3 (04) :208-211
[7]   BENIGN INFANTILE EPILEPSY WITH COMPLEX PARTIAL SEIZURES [J].
WATANABE, K ;
YAMAMOTO, N ;
NEGORO, T ;
TAKAHASHI, I ;
ASO, K ;
MAEHARA, M .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1990, 7 (03) :409-416
[8]   BENIGN PARTIAL EPILEPSY WITH SECONDARILY GENERALIZED SEIZURES IN INFANCY [J].
WATANABE, K ;
NEGORO, T ;
ASO, K .
EPILEPSIA, 1993, 34 (04) :635-638