Alkaptonuria is a rare condition in which a person’s urine turns a dark brownish-black color when exposed to air.
AKU; Alcaptonuria; Homogentisic acid oxidase deficiency; Alcaptonuric ochronosis
A defect in the HGD gene causes alkaptonuria.
The gene defect makes the body unable to properly break down certain amino acids (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. If both parents carry the defective gene related to this condition, each of their children has a 25% chance of developing the disease.
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:
- Darkening of the ear
- Dark spots on the white of the eye (
sclera) and cornea
Exams and Tests
A urine test (
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.
The outcome is expected to be good.
- Homogentisic acid also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement.
Coronary artery diseasemay develop earlier in people with alkaptonuria. Kidney stonesand prostate stones may be more common in people with alkaptonuria.
When to Contact a Medical Professional
Call your health care provider if you notice that your own urine or your child’s urine becomes dark brown or black when it is exposed to air.
Genetic counseling is recommended for persons with a family history of alkoptonuria who are considering having children.
A blood test can be done to see if you carry the gene for alkaptonuria.
Prenatal tests (amniocentesis or chorionic villus sampling) can be done to screen a developing baby for this condition if the genetic change has been identified.