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Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion
Anne-Marie Lamhonwah1, Ivo Barić2,3, Jessica Lamhonwah1
1Division of Neurology Department of Pediatrics, and Genetics and Genome Biology Program The Research Institute The Hospital for Sick Children University of Toronto Toronto Ontario M5G 1X8 Canada.
Abstract:
This boy presented with ADHD at 3 years and at 8 years was hyperactive with no documented hypoglycemia and had myopathy, cardiomyopathy, and very low serum carnitine. L-carnitine improved his exercise intolerance, cardiomyopathy, and behavior. Analysis of SLC22A5 revealed a premature stop codon (p.R282*) and a novel in-frame deletion (p.T440-Y449).
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