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Defects in the carnitine transporter (OCTN2), which is coded by the SLC22A5 gene, create primary carnitine deficiency, expressed as low urinary carnitine excretion and low blood and tissues carnitine level, which may be a risk factor of ASD

[DOI] [PubMed] [Google Scholar] Acosta M.F., Muralidhran P., Abrahamson M.D., Grijalva C.L., Carver M., Tang H., Klinger C., Fineman J.R., Black S.M., Mansour H.M

Risperidone remains one of the only FDA-approved antipsychotics for the management of ASD-associated irritability in children aged 5 to 16 [21]

International journal of sport nutrition, 4(3), 280-288

Liver enlargement in response to hepatic enzyme induction is typically associated with hepatocellular hypertrophy and often, transient hepatocyte hyperplasia