Important: This page is general information, not medical advice. It does not recommend or prescribe any treatment. Always consult your doctor or pharmacist before starting, stopping or changing any medicine.
About Amino Acid Metabolism Disorders
Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body. If you have a metabolic disorder, something goes wrong with this process.
One group of these disorders is amino acid metabolism disorders. They include phenylketonuria (PKU) and maple syrup urine disease. Amino acids are "building blocks" that join together to form proteins. If you have one of these disorders, your body may have trouble breaking down certain amino acids. Or there may be a problem getting the amino acids into your cells. These problems cause a buildup of harmful substances in your body. That can lead to serious, sometimes life-threatening, health problems.
These disorders are usually inherited. A baby who is born with one may not have any symptoms right away. Because the disorders can be so serious, early diagnosis and treatment are critical. Newborn babies get screened for many of them, using blood tests.
Treatments may include special diets, medicines, and supplements. Some babies may also need additional treatments if there are complications.
It sits within Metabolic Problems.
When to speak to someone. Reading about a topic cannot tell you whether it applies to you. Speak to a doctor or pharmacist if symptoms are severe, sudden, getting worse, or simply not going away — and seek emergency care immediately for chest pain, breathing difficulty, sudden weakness or confusion, or a serious allergic reaction.
Research on Amino Acid Metabolism Disorders
666 studies areregistered for this condition on ClinicalTrials.gov, the U.S. National Library of Medicine's public registry. A selection is below — the links go straight to the registry entry, not to a summary of ours.
What a registered study does and does not mean. Registration means a study exists and has been declared publicly. It says nothing about whether the treatment being tested works, is safe, or is available to you. Many studies find no benefit — that is what research is for. Never seek out an experimental treatment on the strength of a registry entry alone.
Research currently under way
- A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-181 in Subjects With PhenylketonuriaAgios Pharmaceuticals, Inc.
- Clinical and Laboratory Study of Methylmalonic AcidemiaNational Human Genome Research Institute (NHGRI)
- Natural History of MADDIcahn School of Medicine at Mount Sinai
- Study of AlkaptonuriaNational Human Genome Research Institute (NHGRI)
- Clinical and Basic Investigations Into Hermansky-Pudlak SyndromeNational Human Genome Research Institute (NHGRI)
- Impact Of A Phe-Restricted Diet On Gut Health In Children With PKUBirmingham Women's and Children's NHS Foundation Trust
Research already completed
- Maternal Inborn Errors of Metabolism in Pregnancy: A Pregnancy Registry ProtocolNational Human Genome Research Institute (NHGRI)
- First-in-Human, Multiple Part Clinical Study of JNT-517 in Healthy Participants and in Participants With PhenylketonuriaOtsuka Pharmaceutical Development & Commercialization, Inc.
Study data from ClinicalTrials.gov, a service of the U.S. National Library of Medicine. Retrieved 2026-07-30. Registry entries are supplied by study sponsors and investigators; ClinicalTrials.gov does not verify their scientific validity. PocketsInfo is not affiliated with, and not endorsed by, the NLM or the NIH.
Where to read more
Rather than paraphrase, we point you to the primary sources. Every link below is to a government health agency, a national institute or a recognised medical body — grouped by what you are trying to find out.
Start Here
- Fatty Acid Oxidation DisordersMerck & Co., Inc.
Genetics
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: MedlinePlus GeneticsNational Library of Medicine
- 3-methylcrotonyl-CoA carboxylase deficiency: MedlinePlus GeneticsNational Library of Medicine
- 3-methylglutaconyl-CoA hydratase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Alkaptonuria: MedlinePlus GeneticsNational Library of Medicine
- Aminoacylase 1 deficiency: MedlinePlus GeneticsNational Library of Medicine
- Arginase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Arginine:glycine amidinotransferase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Argininosuccinic aciduria: MedlinePlus GeneticsNational Library of Medicine
- Asparagine synthetase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Beta-ketothiolase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Dihydrolipoamide dehydrogenase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Glutamate formiminotransferase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Glutaric acidemia type I: MedlinePlus GeneticsNational Library of Medicine
- Guanidinoacetate methyltransferase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Hartnup disease: MedlinePlus GeneticsNational Library of Medicine
- Histidinemia: MedlinePlus GeneticsNational Library of Medicine
- Homocystinuria: MedlinePlus GeneticsNational Library of Medicine
- Hyperlysinemia: MedlinePlus GeneticsNational Library of Medicine
- Hypermethioninemia: MedlinePlus GeneticsNational Library of Medicine
- Hyperprolinemia: MedlinePlus GeneticsNational Library of Medicine
- Isobutyryl-CoA dehydrogenase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Isolated sulfite oxidase deficiency: MedlinePlus GeneticsNational Library of Medicine
Clinical Trials
- ClinicalTrials.gov: Amino Acid Metabolism, Inborn ErrorsNational Institutes of Health
Medical subject headings
Clinicians and researchers index this subject under Amino Acid Metabolism, Inborn Errors. These are the terms to use when searching medical literature.
This page is built from the MedlinePlus health topic record for Amino Acid Metabolism Disorders, a service of the U.S. National Library of Medicine (NLM), National Institutes of Health. Information is from MedlinePlus.gov. PocketsInfo is not affiliated with, and is not endorsed by, the NLM or the NIH. Retrieved 30 July 2026.