Ojeda V J, Grainger K M, Day T J
Med J Aust. 1984 Sep 29;141(7):430-3. doi: 10.5694/j.1326-5377.1984.tb132854.x.
Two sisters developed motor neurone disease (MND), which was associated with progressive intellectual impairment in one; they survived for 18 and 24 months, respectively. At necropsy, the features of MND were confirmed, and the demented patient had severe non-specific cerebral atrophy. No evidence of Alzheimer's disease was found. Organic dementia of non-specific type can be associated with up to 15% of the familial cases of MND and with about 2% of the sporadic cases of MND in the Western world.
两姐妹患了运动神经元病(MND),其中一人还伴有进行性智力障碍;她们分别存活了18个月和24个月。尸检时,MND的特征得到证实,患有痴呆症的患者有严重的非特异性脑萎缩。未发现阿尔茨海默病的证据。在西方世界,非特异性类型的器质性痴呆在高达15%的家族性MND病例和大约2%的散发性MND病例中可能会出现。