
doi: 10.1007/bf02825486
pmid: 16567917
Juvenile amytrophic lateral sclerosis (JALS) is a type of motor neuron disease presenting before 25 years of age. It is characterized by a combination of upper and lower motor signs. It may be familial or sporadic. We are reporting a sporadic case of JALS with onset of symptoms at 4 years of age. Diagnostic criteria and a brief review of literature are presented.
Male, Amyotrophic Lateral Sclerosis, Age Factors, Humans, Child
Male, Amyotrophic Lateral Sclerosis, Age Factors, Humans, Child
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