Abstract
Juvenile amyotrophic lateral sclerosis (JALS) is a rare motor neuron disease (MND) characterized by progressive degeneration of upper and lower motor neurons. Symptoms of JALS typically begin before age 25, but often in early childhood. We present the case of an apparently sporadic ALS patient carrying a missense mutation in FUS gene where previous infection of SARS-CoV-2 misled clinical investigations.
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