Facial Onset Motor and Sensory Neuronopathy Syndrome With a Novel TARDBP Mutation

Conclusions: This is the first time that a novel mutation in TARDBP gene was identified in a patient with FOSMN syndrome, which further suggested a link between FOSMN and amyotrophic lateral sclerosis. Our findings widen the spectrum of TARDBP-related motor neuron diseases.
Source: The Neurologist - Category: Neurology Tags: Case Report/Case Series Source Type: research