Tison F, Arne P, Henry P
Service de Neurologie, Hôpital Pellegrin, Bordeaux, France.
J Neurol. 1989 Jul;236(5):307-8. doi: 10.1007/BF00314464.
A 56-year-old woman with coeliac disease developed myoclonus of cortical origin and palatal myoclonus with lesions of subcortical white matter on magnetic resonance imaging. Myoclonus can thus be a prominent feature of coeliac disease encephalopathy. A slight vitamin E deficiency was found but does not satisfactorily explain this myoclonic encephalopathy, which remains of unknown origin.
一名56岁的乳糜泻女性出现了起源于皮质的肌阵挛和腭肌阵挛,磁共振成像显示其皮质下白质有病变。因此,肌阵挛可能是乳糜泻性脑病的一个突出特征。发现有轻微的维生素E缺乏,但这并不能令人满意地解释这种肌阵挛性脑病,其病因仍然不明。