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(Etiology) Carnitine Deficiency Syndrome is a metabolic muscle disease that is characterized by an interference with fat processing needed for the production of energy (fat metabolism that turns fat into energy) Carnitine Deficiency Syndrome can be either primary or secondary: This condition is caused by a genetic defect in the protein (carnitine transporter protein) that is responsible for transporting carnitine into the cell

It arrives in lyophilized form because freeze-drying removes moisture, which dramatically extends stability lyophilized powder can remain stable for up to 3 years when stored properly

(2017) showed that pesticide exposure in the household, in the perinatal period, can be associated with an increased risk of pediatric-MS onset

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Tameire, F