ketoaciduria

It is also called branched chain ketoaciduria.

Branched-chain ketoaciduria: Seizures and severe mental and physical retardation can result if intake of branched-chain amino acids is increased.

Diabetes Mellitus: 38% of diabetic outpatient clinic visits involve hypomagnesemia, probably through renal loss because of glycosuria or ketoaciduria.

Maple syrup urine disease (MSUD), also called branched-chain ketoaciduria, is an autosomal recessive metabolic disorder affecting branched-chain amino acids.

PubMed - Recent literature Online Books - Medical and science texts Scriver's Online Metabolic and Molecular Bases of Inherited Disease (OMMBID): Maple Syrup Urine Disease (Branched-Chain Ketoaciduria)

BCKD deficiency Branched-chain alpha-keto acid dehydrogenase deficiency Branched-Chain Ketoaciduria Ketoacidemia MSUD For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines and How are genetic conditions and genes named?