Alkaptonuria: Introduction, Symptoms, Causes, Lab Diagnosis, and Treatment
Table of Contents
Alkaptonuria is an enzyme deficiency, homogentisic dioxygenase (HGD) rare inherited disorder. It is used to break down a toxic substance called homogentisic acid. Excess of homogentisic acid causes bones and cartilage to become discolored and brittle which causes later osteoarthritis, especially in the spine and large joints. The patient who has this condition also has urine that turns dark brown or black when it is exposed to air (as shown in the above image).
The following are the common symptoms of Alkaptonuria-
There is no specific treatment so far. Rather, treatment is focused mainly on managing symptoms.
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