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Genetic testing of the expecting parents (and related family members) and prenatal diagnosis (molecular testing of the fetus during pregnancy) may help in understanding the risks better during pregnancy If there is a family history of the condition, then genetic counseling will help assess risks, before planning for a child Active research is currently being performed to explore the possibilities for treatment and prevention of inherited and acquired genetic disorders The prevention of Secondary Carnitine Deficiency Syndrome involves suitably treating the underlying metabolic disorder with which it is associated

the identification of neurons that express these enzymes in the rodent cerebral cortex, hippocampus, olfactory bulb, amygdala, and thalamus suggests that ALLO and THDOC can be synthesized locally from precursors within the CNS (94)

Each compound is matched to its optimal delivery route based on its chemistry and target tissue

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