Ontology highlight
ABSTRACT:
SUBMITTER: Al-Ajlouni JM
PROVIDER: S-EPMC7451899 | biostudies-literature | 2020 Dec
REPOSITORIES: biostudies-literature
Al-Ajlouni Jihad M JM Alisi Mohammed S MS Yasin Mohamad S MS Khanfar Aws A Hamdan Mohammad M Halaweh Ahmad Abu AA Al Hawamdeh Hashem H Tayyem Mohammed M Alsbou Mohammad S MS
Arthroplasty today 20200823 4
Alkaptonuria is a rare autosomal recessive metabolic disorder. It is characterized by the accumulation of homogentisic acid in the body due to a lack of enzymes that degrade it. Over time, it results in joint degeneration and eventually leads to ochronosis. Ochronosis refers to bluish-black discoloration of connective and other tissues within the body. In this study, we present 5 distinct cases diagnosed with alkaptonuria. They have undergone 8 total joint replacement surgeries (4 hips and 4 kne ...[more]