Recurrent episodes of coma:: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1

被引:28
作者
Echenne, B [1 ]
Ducros, A
Rivier, F
Joutel, A
Humbertclaude, V
Roubertie, A
Azaïs, M
Bousser, MG
Tournier-Lasserve, E
机构
[1] Hop St Eloi, Serv Neuropediat, F-34295 Montpellier, France
[2] Hop Necker Enfants Malad, INSERM, U25, Paris, France
[3] Hop Lariboisiere, Serv Neurol, F-75475 Paris, France
[4] Hop Lariboisiere, Serv Genet, F-75475 Paris, France
关键词
migraine; familial hemiplegic migraine; coma; epilepsy;
D O I
10.1055/s-2007-973493
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Over a period of ten years, a boy had several episodes of coma, lasting three to five days. Each episode was preceded by hemiparesis or paresthesias, aphasia, headaches and behavioural changes, with subsequent loss of consciousness, Partial seizures occurred during the first episode. A history of migraine or hemiplegic migraine was found in several members of the family, Linkage to chromosome 1q21-23, where a gene for familial hemiplegic migraine has been mapped, was shown in this family.
引用
收藏
页码:214 / 217
页数:4
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