| Literature DB >> 17899092 |
Serpil Bal1, Yasemin Turan, Hikmet Koçyiğit, Alev Gürgan, Sükran Kurtulmuş, Anil Güvenç, Gonca Deniz.
Abstract
Ochronosis is a rare autosomal-recessive disease, characterized by increased homogentisic acid (HGA) and substrates due to deficiency of HGA oxidase. The most common clinical presentations are homogentisic aciduria, blue-black pigment accumulation in collagen tissues, large joint arthropathies and degenerative disk diseases. However, the disease may exert very large spectrum with various system involvements. In this article, a patient who was admitted by progressed musculoskeletal system pains and diagnosed as ochronosis, especially with emerging cardiovascular involvement, was presented.Entities:
Mesh:
Year: 2007 PMID: 17899092 DOI: 10.1007/s00296-007-0456-9
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631