Long Name: Long-Chain Acyl-CoA Dehydrongenase Deficiency

Symptoms: Usually causes a fatal syndrome, in infants, typified by failure to thrive, enlarged liver, enlarged heart, metabolic encephalopathy, and hypotonia.

Cause: Autosomal recessive

Treatment: See Beta-oxidation Defects

Links: https://rarediseases.info.nih.gov/diseases/9700/lcad-deficiency