Results 111 to 120 of about 6,939 (158)

Treatment of Ochronotic Osteoarthropathy and the Evaluation of Selected Lower Limb Muscle Properties, Including the Patellar Tendon: A Case Report and Mini Literature Review. [PDF]

J Clin Med
Jarecki J, Tomczyk-Warunek A, Posturzyńska A, Warda E, Waśko M, Arciszewski K, Tomaszewska E, Muszyński S, Bieniaś J, Ostapiuk M, Skrzypek T, Gągała J.   +11 more
europepmc   +1 more source

Blackish Discoloration of Articular Cartilage during Total Knee Replacement; a Case Report. [PDF]

J Orthop Case Rep
Puthanveetil DE, Subhash VP, Kannu AN, Kavalakkatt K.   +3 more
europepmc   +1 more source

Combined alkaptonuria and osteoporosis contributing to chronic back pain. [PDF]

Endocrinol Diabetes Metab Case Rep
Riegler A, Anand G.
europepmc   +1 more source

Cardiac Manifestations of Alkaptonuria: Aortic Valve Stenosis and Coronary Artery Disease in a 63-Year-Old Patient. [PDF]

JACC Case Rep
Solís Chávez MB, Montero Cruces L, Romiti S, Saiz-Pardo Sanz M, Maroto Castellanos LC.   +4 more
europepmc   +1 more source

Alkaptonuria: Clinical Spectrum of a Diagnosed Case in Bahrain With a Literature Review. [PDF]

Cureus
Alsahlawi Z, Salman LI, Alaradi AM, Hamada F, Alsahlawi HS, Ali ZM.   +5 more
europepmc   +1 more source

Clinical and molecular characteristics of Chinese patients with alkaptonuria: 4-year follow-up of a pediatric patient and literature review. [PDF]

Mol Genet Metab Rep
Qiu X, Liu Y, Shao Y, Mao X, Zhang J, Chen X, Yin X, Sheng H, Li X, Lin Y.   +9 more
europepmc   +1 more source

A shocking intraoperatively diagnosis of ochronotic knee arthropathy: a case report. [PDF]

Ann Med Surg (Lond)
Shashaa MN, Alkarrash MS, Alhasan Y, Kabbany SA, Rezkallah V, Alhamr A, Al-Araje MM.   +6 more
europepmc   +1 more source

Alkaptonuria with Fracture Neck of Femur - A Case Report. [PDF]

J Orthop Case Rep
Paul AJ, John AS, Chandy VJ.
europepmc   +1 more source

Bilateral Hip Arthroplasty for Ochronotic Arthropathy

Clinical Rheumatology, 2000
Ochronosis is a musculoskeletal manifestation of alkaptonuria, a rare hereditary metabolic disorder characterised by the absence of the enzyme homogentisic acid oxidase and associated with various systemic abnormalities related to the deposition of homogentisic acid pigment (ochronotic pigment).
O, Aynaci, C, Onder, A U, Turhan
exaly   +4 more sources

Ochronotic Arthropathy: Structural and Ultrastructural Features

Ultrastructural Pathology, 1994
Fragments of articular cartilage and synovial membrane in a case of ochronosis were studied by light microscopy (LM), polarized light, and transmission electron microscopy (TEM). Granular and/or shard-shaped pigments were observed in the synovia, cartilage, and subchondral tissue, and dispersed pigment was also seen in the synovial fluid.
Paolo Onori, M Melis, Giuseppe Aliberti   +2 more
exaly   +5 more sources