by Cynthia M. Johnson, MA
Homocystinuria is a problem with the metabolism. It causes low levels of a specific enzyme. These enzymes normally help to break down the amino acids methionine and homocysteine. This causes the buildup of these amino acids.
The most common form of homocystinuria is caused by a deficiency of the enzyme cystathionine beta-synthase.
Homocystinuria is a genetic problem. Both parents must have the defective gene in order for the child to develop the condition. A number of genes have been identified such as CBS, MTHFR, MTR, MTRR, and MMADHC.
Homocystinuria is more common in New South Wales, Australia, and Ireland.
If both parents carry the faulty gene, there is a:
The number and severity of symptoms vary. Symptoms may include:
Early treatment is important. Many states require that newborns be screened for homocystinuria. The test usually looks for high levels of methionine. If the test is positive, blood or urine tests can be done to confirm the diagnosis. These tests can detect high levels of methionine, homocysteine, and other sulfur-containing amino acids. Tests to detect an enzyme deficiency may be done as well.
Prenatal diagnosis of homocystinuria is available. It is done with samples taken during an amniocentesis or chorionic villi sample.
To look for potential complications, the following tests may also be done:
There is no specific cure for homocystinuria. Treatment is focused on managing the levels of methionine. It should begin as early as possible. Treatment may include medication and/or a special diet.
Many people respond to high doses of vitamin B6. The supplement will be needed for the rest of your life. A normal dose of folic acid supplement is helpful. Other medications may also be occasionally needed.
A special diet may help people who don't respond to or don't respond fully to vitamin B6 treatment. Starting the diet early in life can help prevent intellectual disability and other complications. In general, the diet:
Genetic counseling is advised for people with a family history of homocystinuria. The counselor will help you determine the risk your child has of developing homocystinuria.
Genetics Home Reference
National Organization for Rare Disorders
Canadian Organization for Rare Disorders
Homocystinuria. Genetics Home Reference website. Available at:
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Updated March 2016. Accessed March 20, 2018.
Homocystinuria. National Organization for Rare Disorders, Inc. website. Available at:
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Published 2015. Accessed March 20, 2018.
Last reviewed March 2018 by EBSCO Medical Review Board Kari Kassir, MD
Last Updated: 5/30/2014
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