Literature DB >> 20809158

[Alkaptonuria. Ochronotic arthropathy caused by hereditary metabolic disease].

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.

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Year:  2010        PMID: 20809158     DOI: 10.1007/s00132-010-1658-5

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  2 in total

1.  [Alcaptonuria; clinical and biochemical study].

Authors:  K SCHREIER; H PLUCKTHUN
Journal:  Z Kinderheilkd       Date:  1952-08

2.  Ochronotic arthritis: case reports and review of the literature.

Authors:  Ercan Cetinus; Ilhan Cever; Cemal Kural; Haldun Erturk; Mustafa Akyildiz
Journal:  Rheumatol Int       Date:  2004-12-03       Impact factor: 2.631

  2 in total
  2 in total

1.  [A 69-year-old patient with brown-black pigmentation of the sclera].

Authors:  D Schmidt
Journal:  Ophthalmologe       Date:  2011-12       Impact factor: 1.059

2.  Alkaptonuria in a middle-aged female.

Authors:  Aref Hosseinian Amiri; Alireza Rafiei
Journal:  Caspian J Intern Med       Date:  2012
  2 in total

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