Branched chain ketoaciduria

Revision as of 21:16, 3 October 2005 by WikiConvertor (Talk)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

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.