Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulation of homogentisic acid, cartilages get a dark discoloration and become brittle and more vulnerable to mechanical stress (Centinus et al. Rheumatol Int 3:127-131, 2004; Hamdi et al. Int Orthop 23:122-125, 1999; Phornphutkul, N Engl J Med 347:2111-2121, 2002; Thacker, Arthroscopy 19:14-17, 2003). This case report is about a patient first diagnosed for ochronosis by arthroscopy of the knee. Her brother was having similar complaints during follow-up. Both patients were prescribed to take glucosamine and chondroitine. Although no report is found in the literature, regarding the success of this therapy in patients with ochronosis, both patients r...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
In this report, a case of a black meniscus with underlying ochronosis is described. Further analysis...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
In this report, a case of a black meniscus with underlying ochronosis is described. Further analysis...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...