Amyotrophic lateral sclerosis, familial type 3: A generally fatal, inherited progressive disease where destruction of motor nerves in the spinal cord and brain stem cause progressive muscle weakness and wasting. Type 3 is characterized late adulthood onset of symptoms which progress slowly over 5 years. It occurs in an autosomal dominant pattern of inheritance. More detailed information about the symptoms, causes, and treatments of Amyotrophic lateral sclerosis, familial type 3 is available below.
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Prognosis for Amyotrophic lateral sclerosis, familial type 3: progression of symptoms usually over about 5 years
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