Literature DB >> 10085494

Aortic stenosis and coronary artery disease caused by alkaptonuria, a rare genetic metabolic syndrome.

M Vavuranakis1, H Triantafillidi, C Stefanadis, P Toutouzas.   

Abstract

Alkaptonuria is a rare metabolic disease in which homogentisic acid deposits occur in various body tissues. We present a case of alkaptonuria which resulted in aortic stenosis and coronary artery disease due to homogentisic acid deposition.

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Year:  1998        PMID： 10085494     DOI： 10.1159/000006863

Source DB:  PubMed          Journal:  Cardiology        ISSN： 0008-6312            Impact factor:   1.869


  3 in total

1.  Does the combination of chondroitin sulfate and glucosamine delay the cartilage destruction in ochronopathy?

Authors:  Onder M Delialioglu; Bulent Daglar; Kenan Bayrakci; Erman Ceyhan; Ugur Gunel
Journal:  Knee Surg Sports Traumatol Arthrosc       Date:  2009-10       Impact factor: 4.342

2.  Cardiovascular manifestations of Alkaptonuria.

Authors:  Stephen J Pettit; Michael Fisher; James A Gallagher; Lakshminarayan R Ranganath
Journal:  J Inherit Metab Dis       Date:  2011-04-20       Impact factor: 4.982

3.  Ochronosis: complicated tear of black meniscus.

Authors:  Onder M Delialioglu; Bulent Daglar; Kenan Bayrakci; Erman Ceyhan; Kerem Tezel; Selim Erekul; Ugur Gunel
Journal:  Knee Surg Sports Traumatol Arthrosc       Date:  2009-09-25       Impact factor: 4.342
  3 in total

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