Results 71 to 80 of about 6,939 (158)

Optimal management of hemophilic arthropathy and hematomas

, 2014
Sébastien Lobet,1,2 Cedric Hermans,1 Catherine Lambert1 1Hemostasis-Thrombosis Unit, Division of Hematology, 2Division of Physical Medicine and Rehabilitation, Cliniques Universitaires Saint-Luc, Brussels, Belgium Abstract: Hemophilia is a ...
Lobet, Sébastien, Cedric Hermans, Sebastien Lobet, Catherine Lambert, Hermans C, Lambert, Catherine, Lobet S, Lambert C, Hermans, Cédric   +8 more
core   +1 more source

Ochronotic arthropathy - A case report.

Orthopedics & Traumatology, 1987
Alcaptonuria is a rare metabolic disease caused by the deficiency of the enzyme homogentisic acid oxidase. We had a case of ochronotic coxarthropathy. It was a fifty-eight-old male. He had suffered from polyarthralgia for thirty years and the coxalgia was gradually increased for the last five years.
Sagara, Takaaki, Yonemura, Kensuke, Mori, Osamu, Kitagawa, Toshio   +3 more
openaire   +2 more sources

Demographic, Phenotypic and Genotypic Features of Alkaptonuria Patients: A Single Centre Experience

Journal of Pediatric Research, 2018
Aim:Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by a deficiency of homogentisate 1,2-dioxygenase. This enzyme converts homogentisic acid (HGA) into maleylacetoacetic acid in the tyrosine degradation pathway.
Sebile Kılavuz, Fatma Derya Bulut, Deniz Kör, Berna Şeker Yılmaz, Sibel Başaran, Tunay Sarpel, Neslihan Önenli Mungan   +6 more
doaj   +1 more source

Shoulder arthroplasty in alkaptonuric arthropathy: A clinical case report and literature review

, 2012
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting from deficiency of the enzyme homogentisic acid oxidase.
Porcellini, Giuseppe, Pegreffi, Francesco, BELLETTI, Lorenza, Dave, Arpit C., Merolla, Giovanni   +4 more
core   +1 more source

Ochronotic arthropathy in alkaptonuria

Rheumatology, 2020
M Adam, Ali, Richard, Stratton
openaire   +2 more sources

Total Hip Arthroplasty in Ochronotic Arthropathy: A Case Report. [PDF]

J Orthop Case Rep, 2023
Bhattacharjee S, Ahlawat A, Prasad A, Das RK.   +3 more
europepmc   +1 more source

Ochronosis of the Lumbar Spine: A Case Report and Review of Literature

Journal of Clinical and Diagnostic Research
Alkaptonuria is an uncommon genetic condition inherited in an autosomal recessive pattern, characterised by a disruption in the metabolism of phenylalanine and tyrosine, leading to insufficient levels of the enzyme homogentisate and further causes a ...
Abraham Aleyas, B Vijay Anand, Rishab Chandraprakash, Anooj Pravin Chheda, Ashwin Mathew Kadavil   +4 more
doaj   +1 more source

Psoriatic Patients with Arthropathy Show Significant Expression of Free Hla Class I Heavy Chains on Circulating Monocytes: A Potential Role in the Pathogenesis of Psoriatic Arthropathy

, 2008
Background Surface free heavy chains on monocytes were recently implicated in playing a role in the pathogenesis of several forms of arthritis. Objectives To determine the expression of surface free heavy chains (recognized by monoclonal antibody HC10 ...
TSAI, WEN-CHAN;WU, CHING-SHUANG;YU, CHIA-LI;YU, HSIN-SU, 蔡文展;吳慶軒;余家利;余幸司   +1 more
core  

Ochronotic arthropathy of bilateral hip joints: A case report. [PDF]

World J Clin Cases, 2023
Yap San Min N, Rafi U, Wang J, He B, Fan L.   +4 more
europepmc   +1 more source

A clinical case of ochronosis with involvement of the cardiac valvular apparatus and the musculoskeletal system in an 80-year-old patient

КардиоСоматика
BACKGROUND: Ochronosis is a rare disorder caused by an inherited defect in tyrosine metabolism, in which the biochemical degradation pathway is interrupted at the stage of homogentisic acid formation.
Amina M. Alieva, Irina V. Kovtyukh, Irina E. Baykova, Elvira A. Khachirova, Albina B. Sultangalieva, Alexander A. Melnikov, Igor G. Nikitin   +6 more
doaj   +1 more source