Literature DB >> 8571731

The clinical manifestations of ochronosis: a review.

J F Van Offel1, L S De Clerck, L M Francx, W J Stevens.   

Abstract

Ochronosis is a rare disease caused by an inherited lack of homogentisic acid oxidase. Alkaptonuria is the presence of homogentisic acid in urine. Ochronosis is characterized by the deposition of a dark pigment in tissues rich in collagen. A wide spectrum of clinical manifestations is described. The most important signs are ochronotic arthropathy, ocular and cutaneous pigmentation, genitourinary tract obstruction by ochronotic calculi and cardiovascular ochronosis, especially calcification and stenosis of the aortic valve. The constellation of these clinical signs should suggest the diagnosis which is confirmed by the detection of homogentisic acid in urine. There is no cure for the disease and treatment is based on symptomatic measures.

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Year:  1995        PMID: 8571731     DOI: 10.1080/17843286.1995.11718475

Source DB:  PubMed          Journal:  Acta Clin Belg        ISSN: 1784-3286            Impact factor:   1.264


  4 in total

1.  Cardiac ochronosis: valvular heart disease with dark green discoloration of the leaflets.

Authors:  Ersin Erek; Filip R A Casselman; Hugo Vanermen
Journal:  Tex Heart Inst J       Date:  2004

Review 2.  On the ocular findings in ochronosis: a systematic review of literature.

Authors:  Moritz Lindner; Thomas Bertelmann
Journal:  BMC Ophthalmol       Date:  2014-01-30       Impact factor: 2.209

3.  Ochronosis as an unusual cause of valvular defect: a case report.

Authors:  Andreas Wilke; Dietmar Steverding
Journal:  J Med Case Rep       Date:  2009-11-27

4.  Cervical Spondylotic Myelopathy due to the Ochronotic Arthropathy of the Cervical Spine.

Authors:  Nan Li; Wei Tian; Qiang Yuan; Da He
Journal:  J Korean Neurosurg Soc       Date:  2016-01-20
  4 in total

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