Branched chain ketoaciduria

Branched chain ketoaciduria --> maple syrup urine disease

hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterised by urine that smells like maple syrup.

Retrieved from ""
First | Previous (Branched chain acyl-coa oxidase) | Next (Branched chain ketonuria) | Last
Please contribute to this project, if you have more information about this term feel free to edit this page.