Systemic primary carnitine deficiency (SPCD) is an autosomal recessive inborn error of fatty acid metabolism caused by a defect in the transporter responsible for moving carnitine across plasma membrane. The clinical features of SPCD vary widely based on the age of onset and organs involved. During infancy. patients might show episodes of hypoketotic hypoglycemia. https://cosmeticssquadets.shop/product-category/food-items/