Results 81 to 90 of about 6,939 (158)

Reverse total shoulder arthroplasty for treatment of ochronotic arthropathy. [PDF]

J Surg Case Rep, 2022
Butterfield BP, Garver TH.
europepmc   +1 more source

Rapidly progressive osteoarthrosis of ochronotic origin. A pathologic study.

, 1988
A case of hip osteoarthrosis associated with ochronosis in a 65-year-old woman is reported. Characteristic features of both conditions were observed macroscopically and on light and electron microscopic examination.
Baud CA, Cunningham T, Lagier R, Lacotte D   +3 more
core   +1 more source

One-stage revision arthroplasty in a patient with ochronotic arthropathy accompanied by joint infection: A case report. [PDF]

World J Clin Cases, 2022
Wang XC, Zhang XM, Cai WL, Li Z, Ma C, Liu YH, He QL, Yan TS, Cao XW.   +8 more
europepmc   +1 more source

Homogentisate 1,2 dioxygenase is expressed in human osteoarticular cells: implications in alkaptonuria.

, 2012
Alkaptonuria (AKU) results from defective homogentisate1,2-dioxygenase (HGD), causing degenerative arthropathy. The deposition of ochronotic pigment in joints is so far attributed to homogentisic acid produced by the liver, circulating in the blood and ...
LASCHI, MARCELLA, Lia Millucci, SPREAFICO, ADRIANO, Enrico Selvi, TINTI, LAURA, Selvi E., Loredana Amato, BRACONI, DANIELA, BERNARDINI, GIULIA, AMATO, LOREDANA, Annalisa Santucci, Laura Tinti, SANTUCCI, ANNALISA, Daniela Braconi, Giulia Bernardini, GHEZZI, LORENZO, MILLUCCI, LIA, Marcella Laschi, Lorenzo Ghezzi, Adriano Spreafico   +19 more
core   +1 more source

Clinical and Surgical Insights on Bilateral Total Knee Arthroplasty in Ochronotic Arthropathy: A Case-based Review. [PDF]

J Orthop Case Rep, 2021
Saini MK, Reddy NR, Reddy PJ, Reddy CD, Saini N.   +4 more
europepmc   +1 more source

Secondary osteoarthritis due to alkaptonuria: a case report [PDF]

Journal of Research in Applied and Basic Medical Sciences
Background & Aims: Alkaptonuria is a rare autosomal recessive genetic disorder caused by a deficiency of homogentisate 1,2-dioxygenase, leading to the accumulation of homogentisic acid.
Sabina Lois, Aruna Veeruswamy, Kamalanathan Kulandaivelu, Mohan Prasad Muthusamy, Yee Tun Oo   +4 more
doaj  

Black joint and synovia: Histopathological evaluation of degenerative joint disease due to Ochronosis

, 2015
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.
Doganavsargil, Basak, ÇOKER, MAHMUT, ARGIN, MEHMET, Pehlivanoglu, BURÇİN, Bingul, Kenan Baris, Kececi, Burcin, SEZAK, MURAT, Oztop, Fikri, KAYA BİÇER, MELEKPER ELCİL   +8 more
core   +1 more source

Acute Anterior Uveitis as the Initial Presentation of Alkaptonuria

, 2009
Alkaptonuria is a rare autosomal recessive metabolic disorder that may present with multi-system involvement such as ochronotic arthropathy, renal, urethral and prostatic calculi, cardiac valvular lesions and pigmentation of the skin, sclera, cartilage ...
David, S., Padhan, P., John, S.S., Mathews, J.V.   +3 more
core   +2 more sources

Hip arthroplasty for ochronosis

, 2005
Alkaptonuria is a metabolic disorder in which homogentisic acid oxidase is absent. Therefore, homogentisic acid accumulates in cartilage and connective tissues.
Kerimoglu, SERVET, ONDER, C, AYNACI, OSMAN, MALKOC, CH   +3 more
core  

Total Knee Arthroplasty in Alkaptonuric Patient With Ochronotic Arthropathy. [PDF]

J Am Acad Orthop Surg Glob Res Rev
Michalak P, Buchcic P, Drobniewski M, Borowski A.   +3 more
europepmc   +1 more source