Motor neuron disease (amyotrophic lateral sclerosis) arising from longstanding primary lateral sclerosis.
نویسندگان
چکیده
Three men were initially diagnosed as having primary lateral sclerosis (PLS), but eventually developed amyotrophic lateral sclerosis (ALS) after 7.5, 9, and at least 27 years. Non-familial ALS and PLS might be different manifestations of a single disease or constitute completely distinct entities. The clinical diagnosis of PLS predicts a median survival that is four to five times longer than in ALS.
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ورودعنوان ژورنال:
- Journal of neurology, neurosurgery, and psychiatry
دوره 58 6 شماره
صفحات -
تاریخ انتشار 1995