Bilateral hip arthroplasty for ochronotic arthropathy

Aynaci O., Onder C. , Turhan A.

CLINICAL RHEUMATOLOGY, cilt.19, sa.2, ss.150-152, 2000 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 19 Konu: 2
  • Basım Tarihi: 2000
  • Doi Numarası: 10.1007/s100670050035
  • Sayfa Sayıları: ss.150-152


Ochronosis is a musculoskeletal manifestation of alkaptonuria, a rare hereditary metabolic disorder characterised by the absence of the enzyme homogentisic acid oxidase and associated with various systemic abnormalities related to the deposition of homogentisic acid pigment (ochronotic pigment). In this report, we describe a 53-year-old, HLA-B27(+) woman with ochronotic arthropathy. In addition to the typical clinical features of the disorder, she had bilateral hip involvement, which was improved by cementless total hip prosthesis.