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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

(EI 866/2-1)

Similarly, the LIP-deficient C/EBP uORF MEFs maintained lower NADH/NAD + ratios, while ectopic expression of LIP in wt MEFs increased the NADH/NAD + ratio