In this report, a case of a black meniscus with underlying ochronosis is described. Further analysis by laboratory findings showed that the patient had underlying alkaptonuria, which was previously undiagnosed. The patient’s symptoms showed improvement after arthroscopic treatmen
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...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
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 ...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
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...
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...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
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 ...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
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...
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...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
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