Alkaptonuria: Introduction, Symptoms, Causes, Lab Diagnosis, Treatment, and Keynotes
Introduction 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 …
