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To date, the carnitine deficiency phenotype was observed in the context of (a) primary carnitine deficiency resulting from inactivating mutations in Octn2 gene, (b) secondary carnitine deficiency that may be caused by different metabolic abnormalities all ultimately leading to the loss of carnitine in the urine, and (c) patients with CKD undergoing hemodialysis and losing carnitine through the dialysis membrane (reviewed in ref

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Transcription factors in neurodevelopmental and associated psychiatric disorders: a potential convergence for genetic and environmental risk factors

Adam Maddox Medical Director A graduate from Northern Arizona University and the National College of Naturopathic Medicine, Dr