Results 11 to 20 of about 7,435 (127)

Knee Arthroscopy: A Diagnostic and Therapeutic Tool for Management of Ochronotic Arthropathy [PDF]

open access: yesArthroscopy Techniques, 2018
The surgical treatment of ochronotic arthropathy remains unclear. Although there is no absolute cure for ochronotic arthropathy, current management typically begins with conservative treatment.
William B. Stetson, M.D.   +3 more
doaj   +4 more sources

Ochronotic arthropathy effectively treated with total hip and total knee arthroplasty: a case report [PDF]

open access: yesFrontiers in Medicine, 2023
Ochronosis is a rare autosomal recessive disorder of tyrosine metabolism characterized by multilevel spinal degeneration and arthritis of large weight-bearing joints, which is referred to as ochronotic arthropathy.
Yikai Liu   +4 more
doaj   +4 more sources

Patients with Black Hip and Black Knee Due to Ochronotic Arthropathy: Case Report and Review of Literature [PDF]

open access: yesOman Medical Journal, 2013
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.
Mehmet Ali Acar   +5 more
doaj   +4 more sources

Long-term result of arthroplasty in the treatment of a case of ochronotic arthropathy [PDF]

open access: yesActa Orthopaedica et Traumatologica Turcica, 2016
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.
Sinan Karaoğlu   +2 more
doaj   +3 more sources

Total hip arthroplasty in patients with alkaptonuria: a case report [PDF]

open access: yesFrontiers in Surgery
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by mutations in the homogentisate 1,2-dioxygenase (HGD) gene, often leading to debilitating ochronotic arthropathy that requires total joint arthroplasty (THA). This case report describes a
Bo Zhu   +3 more
doaj   +3 more sources

Case Report: First Documented Hip Arthroplasty on Chinese Patient with Ochronotic Arthropathy [PDF]

open access: yesFrontiers in Surgery, 2022
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by homogentisc acid (HGA) accumulation, the deposition of which in the joints usually causes ochronotic arthropathy.
Zhibo Ying   +5 more
doaj   +2 more sources

Case Report: Ochronotic Arthropathy [PDF]

open access: yesForbes Tıp Dergisi, 2021
Ochronosis is a rare metabolic disease caused by the deficiency of the homogentisic acid oxidase enzyme. It gives clinical findings related to the accumulation of homogentisic acid in soft tissues and excretion in urine. Patients with chronic arthropathy
Ülkü Dönmez   +3 more
doaj   +2 more sources

Direct repair of the chronic ochronotic Achilles tendon rupture: a case report [PDF]

open access: yesBMC Musculoskeletal Disorders
Background Alkaptonuria (AKU) is a rare hereditary disease. Ochronotic arthropathy, tendinopathy, and osteopenia/osteoporosis are generally musculoskeletal manifestations in patients with AKU.
Takuji Yokoe   +6 more
doaj   +3 more sources

Ochronotic arthropathy mimicking degenerative osteoarthritis in an older adult with alkaptonuria: diagnostic and perioperative lessons from a case report [PDF]

open access: yesFrontiers in Medicine
BackgroundAlkaptonuria is a rare inherited metabolic disorder caused by impaired homogentisic acid metabolism. Ochronotic arthropathy is a late musculoskeletal manifestation and may mimic ordinary degenerative osteoarthritis in older adults.
Yong-Ming Zhang   +3 more
doaj   +2 more sources

Total Hip Arthroplasty in Ochronotic Arthropathy with quadriceps tear. A Case Report with a Review of the Literature [PDF]

open access: yesJournal of Orthopaedic Case Reports
Introduction: Alkaptonuria is a rare genetic disorder characterized by the absence of the enzyme homogentisate 1,2 dioxygenase, which leads to the accumulation of homogentisic acid in connective tissues and blood, resulting in Ochronosis and ...
Alok Chandra Agrawal   +4 more
doaj   +2 more sources

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