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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

Lecithin breaks down and removes unnecessary fat cells

Mimo e organizm sam jest w stanie wyprodukowa L-karnityn, to potrzebuje do tego kilku wanych mikroelementw, w tym witaminy B6, witaminy C, niacyny, elaza i metioniny

The typical symptoms include numbness and tingling, weakness, and burning or stabbing pain

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