AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites of oxidation and polymerization of homogentisic acid, which have high affinity to collogen, in the connective tissues. It is a clinical condition characterized with ochronotic pigmentation of tissues, degenerative arthropathy of especially large joints and black discoloration of urine. In this paper we present a case of ochronosis diagnosed with biopsy and additional tests when a black discoloration of menisci and joint cartilage were detected during arthroscopic intervention for a degenerative meniscus tear.PRESENTATION OF CASEA forty two year-old male patient was operated for lateral meniscus tear of his right knee. The arthroscopic examina...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Alkaptonuria is a rare autosomal recessive disorder characterised by the absence of homogentisic aci...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
In this report, a case of a black meniscus with underlying ochronosis is described. Further analysis...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
WOS: 000355639400008PubMed ID: 25869213Introduction: Ochronotic arthropathy is a rapidly progressive...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Ochronosis is dark pigmentation of connective tissue in patients with alkaptonuria. The dark pigment...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Alkaptonuria is a rare autosomal recessive disorder characterised by the absence of homogentisic aci...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
In this report, a case of a black meniscus with underlying ochronosis is described. Further analysis...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
WOS: 000355639400008PubMed ID: 25869213Introduction: Ochronotic arthropathy is a rapidly progressive...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Ochronosis is dark pigmentation of connective tissue in patients with alkaptonuria. The dark pigment...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Alkaptonuria is a rare autosomal recessive disorder characterised by the absence of homogentisic aci...