Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic acid oxidase, which results in excess homogentisic acid (HGA) levels. Homogentisic acid and its oxidation products can accumulate in hyaline cartilage, tendons, and ligaments. A 55-year-old male was admitted complaining of worsening chronic pain in his left knee. A radiographic evaluation showed tricompartmental end- stage osteoarthritis. A cemented total knee replacement was performed. At the 10-year follow-up, he had returned to full activity, had no knee pain, and was very satisfied with the outcome. No abnormality was observed in the femoral, tibial, or patellar components on radiography. We believe that total knee replacement is a good opti...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Objective: Unusual or unexpected effect of treatment Background: Ochronosis is an inherited metaboli...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
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 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...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Objective: Unusual or unexpected effect of treatment Background: Ochronosis is an inherited metaboli...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria is a rare metabolic disease in which a deficiency of the enzyme homogentisate dioxygena...
WOS: 000087735500023PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized...
PubMed ID: 10884219Alkaptonuria is an inherited metabolic disorder characterized by the absence of t...
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 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...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Ochronotic arthropathy is a rare condition found in patients with alkaptonuria. Due to the accumulat...
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is d...
Objective: Unusual or unexpected effect of treatment Background: Ochronosis is an inherited metaboli...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...