Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly.
Important It is possible that the main title of the report Maple Syrup Urine Disease is not the name you expected. Please check the synonyms listing to ...
Maple syrup urine disease (MSUD) is a rare, inherited metabolic disorder. With MSUD, the body cannot break down certain amino acids. Individuals who have the disease ...
Maple syrup urine disease (MSUD) is an aminoacidopathy secondary to an enzyme defect in the catabolic pathway of the branched-chain amino acids leucine ...
Maple syrup urine disease (MSUD), also called branched-chain ketoaciduria, is an autosomal recessive  metabolic disorder affecting branched-chain amino acids.
MSUD is inherited in an autosomal recessive pattern. For a child to get the disease, he or she must inherit a defective copy of the gene from each parent.
Understanding maple syrup urine disease, a genetic disorder involving high blood amino acid levels causing a characteristic urine smell.
Maple syrup urine disease (MSUD) is a condition in which the body is unable to break down certain proteins. The condition is named for the sweet odor of the urine of ...
Maple syrup urine disease (MSUD) is a disorder in which the body cannot break down certain parts of proteins. The urine of people with this condition can ...
Maple syrup urine disease (MSUD) is classified as classic or intermediate. Twelve hours after birth, untreated neonates with classic MSUD have a maple syrup odor in ...