We report a case of a 35-year-old male who has ochronotic arthropathy involving his
spine and peripheral joints. He was diagnosed as having Alkaptonuria,which is a rare
disorder of tyrosine catabolism with an autosomal recessive trait. (Rawal Med J
2006;31:46-47)
Key words: alkaptonuria, ochronosis, inborn error of metabolism
The articles in Bibliomed are open access articles licensed under Creative Commons Attribution 4.0 International License (CC BY), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.