AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase characterized by excretion of homogentisic acid in urine, deposition of oxidized homogensitate pigments in connective tissues and articular cartilages (ochronosis). The result is dark pigmentation and weakening of the tissues resulting in chronic inflammation and osteoarthritis. Management of alkaptonuric ochronic osteoarthritis is usually symptomatic and replacements have comparable outcomes to osteoarthritis in patients without ochronosis. I report a case of a patient with ochronosis of knee treated with total knee replacement and report operative pearls for surgery in this rare disorder
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
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...
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...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
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...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
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...
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...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
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...
INTRODUCTION Ochronosis is a rare disorder which is defined as the deposition of metabolites of oxid...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
AbstractINTRODUCTIONOchronosis is a rare disorder which is defined as the deposition of metabolites ...