Publications by authors named "Vamseedhar A"
Indian J Clin Biochem
April 2010
Article Synopsis
- Alkaptonuria is a rare genetic disorder that leads to the buildup of homogentisic acid due to the lack of a specific enzyme, causing physical symptoms over time.
- The case study details a 55-year-old man who experienced stroke-like symptoms, arthritis, and changes in urine color, prompting further investigation.
- Biochemical tests confirmed alkaptonuria and revealed associated complications such as mild kidney issues and crystal formation in urine, highlighting the rarity of such complications in previous reports.
