Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accumulation of pigment deposits of homogentisic acid in the joint cartilage results in ochronotic osteoarthritis. We present a case of a 62-year-old female who underwent staged left uncemented total hip and right cemented total knee arthroplasty for osteoarthritis secondary to ochronosis
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...