short-chain acyl-CoA dehydrogenase deficiency (SCAD deficiency)

Pathology

• acute acidosis & muscle weakness in infants
• a form of lipid-storage myopathy in adults

Genetics

• autosomal recessive
• associated with defects in ACADS gene

More general terms

• lipid metabolism, inborn error; lipid storage disease; lipidosis

Database

• OMIM: https://mirror.omim.org/entry/201470