Alkaptonuria

Authors

  • Md Nazrul Islam Junior Consultant, Dept. of Medicine, Khulna Medical College Hospital, Khulna
  • SM Kamal Prof & Head; Dept. of Medicine, Khulna Medical College, Khulna
  • Sk Amir Hossain Prof, Dept. of Medicine, Khulna Medical College, Khulna
  • Sirajul Islam Associate Prof, Dept. of Medicine, Khulna Medical College, Khulna

DOI:

https://doi.org/10.3329/bmjk.v49i1-2.31825

Abstract

Alkaptonuria is a rare metabolic autosomal recessive disorder. It occurs due to lack of an enzyme that results in deposition of homogentisic acid in various tissues. A male patient of 45 years presented with back pain for 20 years and multiple joint pain for 10 years. Patient has multiple nodules in both pinnae and pigmentation in both sclerae. His urine turns black upon standing. These findings are compatible with the diagnosis of Alkaptonuria.

Bang Med J (Khulna) 2016; 49 : 37-39

Downloads

Download data is not yet available.
Abstract
25
PDF
35

Author Biography

Md Nazrul Islam, Junior Consultant, Dept. of Medicine, Khulna Medical College Hospital, Khulna



Downloads

Published

2017-03-07

How to Cite

Islam, M. N., Kamal, S., Hossain, S. A., & Islam, S. (2017). Alkaptonuria. Bangladesh Medical Journal Khulna, 49(1-2), 37–39. https://doi.org/10.3329/bmjk.v49i1-2.31825

Issue

Vol. 49 No. 1-2 (2016)

Section

Case Reports

License

Copyright is normally held by the author of the article.