LCAD
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