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Medium-chain Acyl-COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment.

Emily MasonCharles C T HindmarchKimberly J Dunham-Snary
Published in: Endocrinology, diabetes & metabolism (2022)
MCADD is a commonly inherited metabolic disease with serious implications for health outcomes, particularly in children, that may be successfully managed with proper intervention.
Keyphrases
  • fatty acid
  • randomized controlled trial
  • young adults