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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

Eur J Psychotraumatol

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The oxidising ratio of trimethylamine N-oxide was reduced in all three patients before and after treatment, although these changes were not statistically significant [31]

Pediatr Neurol 1993;9:187-193

SREBP-1a is a splice variant of SREBP-1 and has a minor role in activating transcription of cholesterol and lipogenic genes (292)