<--- Back to Details
First PageDocument Content
Biology / Maple syrup urine disease / Branched-chain alpha-keto acid dehydrogenase complex / Inborn error of metabolism / Newborn screening / Branched-chain amino acid / Dihydrolipoamide dehydrogenase / Propionic acidemia / Methylmalonic acidemia / Health / Rare diseases / Medicine
Date: 2007-06-25 16:37:12
Biology
Maple syrup urine disease
Branched-chain alpha-keto acid dehydrogenase complex
Inborn error of metabolism
Newborn screening
Branched-chain amino acid
Dihydrolipoamide dehydrogenase
Propionic acidemia
Methylmalonic acidemia
Health
Rare diseases
Medicine

Microsoft Word - msud_ref

Add to Reading List

Source URL: www.idph.state.ia.us

Download Document from Source Website

File Size: 33,33 KB

Share Document on Facebook

Similar Documents

Medicine / Maple syrup urine disease / BCKDHB / Newborn screening / Leucine / Thiamine / Organic acidemia / Hypoglycemia / Branched-chain alpha-keto acid dehydrogenase complex / Health / Rare diseases / Chemistry

Maple Syrup Urine Disease (MSUD) What is maple syrup urine disease (MSUD)? Maple syrup urine disease (also known as MSUD) is an inherited condition that affects the way a person’s body uses certain parts of protein. A

DocID: HaGa - View Document

Branched-chain amino acids / Rare diseases / Essential amino acids / Ketogenic amino acids / Proteinogenic amino acids / Maple syrup urine disease / Branched-chain alpha-keto acid dehydrogenase complex / Leucine / Medical genetics / Medicine / Health / Chemistry

Maple Syrup Urine Disease (MSUD) (metabolic condition: amino acid disorder) Also known as: • branched-chain alpha-keto acid dehydrogenase deficiency • branched-chain ketoaciduria

DocID: EgrP - View Document

Organic chemistry / Branched-chain amino acids / Maple syrup urine disease / Essential amino acids / Ketogenic amino acids / Proteinogenic amino acids / Branched-chain alpha-keto acid dehydrogenase complex / Health / Rare diseases / Chemistry

MAPLE SYRUP URINE DISEASE

DocID: Ee5e - View Document

Biology / Maple syrup urine disease / Branched-chain alpha-keto acid dehydrogenase complex / Inborn error of metabolism / Newborn screening / Branched-chain amino acid / Dihydrolipoamide dehydrogenase / Propionic acidemia / Methylmalonic acidemia / Health / Rare diseases / Medicine

Microsoft Word - msud_ref

DocID: zjDD - View Document

Autoantigens / Pediatrics / Branched-chain amino acids / Maple syrup urine disease / Branched-chain alpha-keto acid dehydrogenase complex / Newborn screening / Dihydrolipoamide dehydrogenase / Pyruvate dehydrogenase / Inborn error of metabolism / Health / Rare diseases / Medicine

Disease Name MAPLE SYRUP URINE DISEASE (MSUD) (BRANCHED-CHAIN KETOACIDURIA; BRANCHED-CHAIN ALPHA-KETO ACID DEHYDROGENASE DEFICIENCY; MSUD; KETO ACID DECARBOXYLASE DEFICIENCY) Organic aciduria Classification:

DocID: xUdG - View Document