| Literature DB >> 19242077 |
S S John1, P Padhan, J V Mathews, S David.
Abstract
Alkaptonuria is a rare autosomal recessive metabolic disorder that may present with multi-system involvement such as ochronotic arthropathy, renal, urethral and prostatic calculi, cardiac valvular lesions and pigmentation of the skin, sclera, cartilage and other connective tissues. An association of the disease with uveitis has never been reported. We report the first case of alkaptonuria with ochronotic arthropathy presenting with recurrent acute anterior uveitis as the initial manifestation. The possible common link with the HLA-B27 gene is discussed.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19242077 DOI: 10.4103/0022-3859.48438
Source DB: PubMed Journal: J Postgrad Med ISSN: 0022-3859 Impact factor: 1.476