ICD E71.0ORPHA:511MSUD

Maple Syrup Urine Disease

Maple syrup urine disease is a rare inherited disorder in which the body cannot fully break down certain amino acids from protein. These build up in the blood and can harm the brain, causing poor feeding, sleepiness and a sweet smell to the urine. Care involves a special low-protein diet, regular blood monitoring and urgent treatment during illness.

300
Articles
9
Trials
Updated
24 September 2026
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Common Questions

What is Maple Syrup Urine Disease?

Maple syrup urine disease is a rare inherited disorder in which the body cannot fully break down certain amino acids from protein. These build up in the blood and can harm the brain, causing poor feeding, sleepiness and a sweet smell to the urine. Care involves a special low-protein diet, regular blood monitoring and urgent treatment during illness.

How many clinical trials are available for Maple Syrup Urine Disease?

RareWays currently indexes 9 clinical trials for Maple Syrup Urine Disease, of which 1 is actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Maple Syrup Urine Disease come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.