| Literature DB >> 20809158 |
A Klein1, H-W Körner, F Schulz.
Abstract
Alkaptonuria is a rare hereditary metabolic disease. We report the case of a 72-year-old woman who suffered from pain and limitation of motion in the major joints and spine since middle age because of osteoarthrosis deformans alkaptonurica.During knee replacement typical black coloration were detected. Early therapy can reduce disease progression but there is no way to heal alkaptonuria.Entities:
Mesh:
Year: 2010 PMID: 20809158 DOI: 10.1007/s00132-010-1658-5
Source DB: PubMed Journal: Orthopade ISSN: 0085-4530 Impact factor: 1.087