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There are a bunch of other inborn errors of metabolism, including short-chain acyl-CoA dehydrogenase deficiency and medium-chain acyl-CoA dehydrogenase deficiency.[ref] Lets look at the inborn errors of metabolism involving carnitine: CPT2 gene: The CPT2 gene encodes the enzyme that moves fatty acids attached to carnitine into the inner membrane of the mitochondria
While the stunted growth is often viewed as a pathological outcome, it may also reflect adaptive responses to environmental stress, including dietary excess
Related codes to consider before using H57.9 Before defaulting to H57.9, check whether any of these more specific codes applies
Temporarily lowering the dose then ramping back up
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