![]() |
![]() |
AlkaptonuriaDefinition Alkaptonuria is a rare inherited disorder of metabolism, characterized by urine that turns black when exposed to air. Another characteristic is the development of arthritis in adulthood. Causes, incidence, and risk factors Alkaptonuria is an autosomal recessive inherited disorder. In affected individuals, an amino acid known as tyrosine is not properly metabolized, due to a defect in an enzyme called homogentisic acid oxidase. Because of the defect, homogentisic acid is excreted in the urine and turns a brown color upon exposure to air. This is the result of a dark pigment with an ochre color (earthy red or yellow), which led to the name ochronosis. The bones and cartilage of the body may be brown-colored. Symptoms Infant or child:
Signs and tests Urinalysis is positive for reducing substance. Further urine testing shows a positive ferric chloride test. Treatment Some patients benefit from high-dose vitamin C. This has been shown to decrease the build-up of brown pigment in the cartilage, which may slow the rate of development of arthritis. Expectations (prognosis) The outcome is expected to be good. Complications
Calling your health care provider 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 Like most genetic diseases, alkaptonuria itself cannot be prevented, but some of the manifestations, such as arthritis, can be minimized by treatment. Page Content: Alcaptonuria; Homogentisic acid oxidase deficiency; Ochronosis ; ochronosis; exogenous ochronosis; alcaptonuria |
![]() ![]() ![]() |