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CTD is also called: Systemic primary carnitine deficiency (SPCD) Systemic carnitine deficiency (SCD) Primary carnitine deficiency Carnitine uptake defect (CUD) WHERE CAN I FIND MORE INFORMATION

This condition is inherited in an autosomal recessive manner Secondary Carnitine Deficiency Syndrome can also occur, in which case it develops because of other metabolic disorders in the body Autosomal recessive: Autosomal recessive conditions are traits or disorders that occur when two copies of an abnormal gene have been inherited on a non-sex chromosome

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As shown in Table 3, rosuvastatin, simvastatin, and atorvastatin have been approved for the treatment of high cholesterol, atherosclerosis, and diabetes, with significant lipid-lowering effects that effectively reduce LDL levels and decrease the occurrence of cardiovascular events

Carnitine exists in two isomeric forms: L-Carnitine and D-Carnitine, of which L-Carnitine is the physiological active form