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Future perspectives The main limitation of using E

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OMIM: 607483) is a neurometabolic autosomal recessive disorder caused by a mutation in the SLC19A3 gene, characterized by subacute encephalopathy with confusion, convulsions, muscle rigidity, ataxia, dysarthria, and dystonia, which can be fatal if left untreated

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Cohort 1 During the 21-day follow-up period, there were only four cases of SARS-CoV-2 infection in Cohort 1, evenly distributed between the LCLT ( n = 2) and placebo ( n = 2) groups and, therefore, the majority of the participants remained free of COVID-19 during the follow-up period

Moss & Shaffer, 2017)