Abstract

Alkaptonuria is a rare metabolic disease leading to the accumulation of a blue-black pigment namely homogentisic acid in the cartilaginous tissue and body fluids giving them a black color. It is an autosomal recessive disease due to the deficiency of the hepatic enzyme oxidase which results in the accumulation of homogentisic acid in the skin, cartilage, and collagenous tissue giving them a black color. Herein we report a case of 65 years old gentleman who presented to our emergency department post domestic fall on his left hip, after which pain and swelling developed around the left hip and he was unable to bear weight with restricted mobility around the same.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.