Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygenase causes an accumulation of homogentisic acid. Ochronosis consists of excessive deposition of homogentisic acid in the connective tissue and presents as a chestnut brown or black pigmentation. With aging, the accumulation of pigments from homogentisic acid in the joints causes osteoarthrosis. There is no specific treatment for the disease and the approach is symptomatic. Arthroplasty is the solution for severe cases of osteoarthrosis caused by this pathological condition and presents results comparable to those from patients with primary osteoarthrosis. Here, the case of a 67-year-old patient who underwent several arthroplasty procedures bec...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
Alkaptonuria (AKU) is a rare autosomal recessive condition with a prevalence of 1 in 250 000–1 000 0...
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...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
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...
Alkaptonuria (AKU) is a rare autosomal recessive condition with a prevalence of 1 in 250 000–1 000 0...
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...
AbstractAlkaptonuria is disorder of tyrosine metabolism due to deficiency of homogentisic oxidase ch...
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic aci...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is an autosomal recessive disorder caused by the deficiency of homogentisate 1.2 dioxyg...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
Ochronotic arthropathy is a manifestation of longstanding alkaptonuria. With increasing age, an accu...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
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...
Alkaptonuria (AKU) is a rare autosomal recessive condition with a prevalence of 1 in 250 000–1 000 0...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...