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Alternative Names
AKU; Alcaptonuria; Homogentisic acid oxidase deficiency; Alcaptonuric ochronosisDefinition Return to top
Alkaptonuria is a rare condition in which a person's urine turns a dark brownish-black color when exposed to air.
See also: Inborn error of metabolism
Causes Return to top
A defect in the HGD gene causes alkaptonuria.
The gene defect makes the body unable to properly break down certain proteins (tyrosine and phenylalanine). As a result, a substance called homogentisic acid builds up in the skin and other body tissues. The acid leaves the body through the urine. The urine turns brownish-black when it mixes with air.
Alkaptonuria is inherited, which means it is passed down from parents to their children. To get this disease, each of your parents must pass you a copy of the faulty HGD gene.
Symptoms Return to top
Urine in an infant's diaper may darken and can turn almost black after several hours. However, many persons with this condition may not know they have it until mid-adulthood, around age 40, when joint and other problems occur.
Symptoms may include:
Exams and Tests Return to top
A urine test (urinalysis) is done to test for alkaptonuria. If ferric chloride is added to the urine, it will turn the urine a black color in patients with this condition.
Treatment Return to top
Some patients benefit from high-dose vitamin C. This has been shown to decrease the build up of brown pigment in the cartilage and may slow the development of arthritis.
Outlook (Prognosis) Return to top
The outcome is expected to be good.
Possible Complications Return to top
People with this condition also can get arthritis in adulthood. The build-up of homogentisic acid in the cartilage causes arthritis in about 50% of older adults with alkaptonuria.
When to Contact a Medical Professional Return to top
Call your health care provider if you notice that your own urine or your child's urine becomes dark brown or black upon exposure to air.
Prevention Return to top
There is no know prevention.
Update Date: 7/2/2007 Updated by: Brian Kirmse, M.D., Department of Human Genetics, Mount Sinai School of Medicine, New York, NY. Review provided by VeriMed Healthcare Network.
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Page last updated: 02 January 2008 |