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Case Reports
. 2008 Jun;31(6 Pt 1):624.

[Ocular ochronosis. A case report]

[Article in French]
Affiliations
  • PMID: 18772817
Case Reports

[Ocular ochronosis. A case report]

[Article in French]
N Ben Rayana et al. J Fr Ophtalmol. 2008 Jun.

Abstract

Ochronosis or alkaptonuria is a rare inherited disease. It is characterized by the deposition of dark pigments in collagen-rich tissues, which leads to clinical manifestations such as arthropathy. The ochronotic pigment can be found in the sclera, the conjunctiva, and the limbic cornea. Vision is usually not affected. We report the case of 47-year-old patient who complained of lower back pain. Ophthalmologic examination showed dark pigments in the conjunctiva. The increased levels of homogentisic acid in urine confirmed the diagnosis of ochronosis.

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