Introduction: Ochronotic arthropathy is a rapidly progressive and disabling arthropathy predominantly encountered after the fifth decade of life, caused by homogentisate1,2 dioxygenase enzyme deficiency. As it is rare disease, the literature on histological findings is fragmented
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Introduction: Ochronotic arthropathy is a rapidly progressive and disabling arthropathy predominantl...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
Endogenous ochronosis (EO) or alkaptonuria is an inherited autosomal recessive disease caused by the...
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...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Introduction: Ochronotic arthropathy is a rapidly progressive and disabling arthropathy predominantl...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
AbstractAlkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate d...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...
Endogenous ochronosis (EO) or alkaptonuria is an inherited autosomal recessive disease caused by the...
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...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...