Results 21 to 30 of about 209 (127)

Cartilage icing and chondrocalcinosis on knee radiographs in the differentiation between gout and calcium pyrophosphate deposition.

open access: yesPLoS ONE, 2020
OBJECTIVE:To determine if findings of "cartilage icing" and chondrocalcinosis on knee radiography can differentiate between gout and calcium pyrophosphate deposition (CPPD).
Anna L Falkowski   +6 more
doaj   +1 more source

Orthostatic hypotension as an unusual presentation of spinal calcium pyrophosphate deposition disease: case report and review of literature

open access: yesRomanian Journal of Internal Medicine, 2023
Calcium pyrophosphate crystal deposition disease (CPPD), also known as pseudogout, with spinal involvement, is associated with clinical manifestations of acute nerve compression or chronic spinal stenosis.
De Azevedo Sofia Moura   +5 more
doaj   +1 more source

Heritability of crystal related arthropathies [PDF]

open access: yesRomanian Journal of Rheumatology, 2022
The most common types of crystal arthropathies are gout and calcium pyrophosphate deposition (CPPD) disease. Serum urate levels are influenced by a combination of genetic factors and the environment. There are studies estimating the heritability of urate
Claudiu Avram   +4 more
doaj   +1 more source

Condrocalcinose articular familiar Familial articular chondrocalcinosis

open access: yesRevista Brasileira de Reumatologia, 2004
Condrocalcinose articular familiar é uma condição clínica caracterizada pela deposição de cristais de pirofosfato de cálcio no líquido sinovial e cartilagens articulares levando à artrite.
Mittermayer Barreto Santiago   +4 more
doaj   +1 more source

Calcium Pyrophosphate Dihydrate Crystal Deposition Disease Involving the Ligamentum Flavum of the Cervical Spine with Intense Enhancement on MRI: A Case Report

open access: yes대한영상의학회지, 2020
Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease is characterized by chondrocalcinosis, which mainly affects the knees, wrists, pelvis, and rarely, the spine.
Junyoung Lee, Seunghun Lee, Jiyoon Bae
doaj   +1 more source

Gitelman syndrome associated with chondrocalcinosis: description of two cases

open access: yesReumatismo, 2011
Gitelman syndrome is a rare inherited tubulopathy, characterized by hypomagnesemia, hypokalemia, metabolic alkalosis, hypocalciuria and hyperreninemic hyperaldosteronism.
E. Filippucci   +7 more
doaj   +1 more source

Calcium pyrophosphate crystal deposition disease as a risk factor for cardiovascular diseases

open access: yesНаучно-практическая ревматология, 2020
Calcium pyrophosphate crystal deposition disease (CPPD) is an inflammatory joint disease associated with abnormal accumulation of inorganic pyrophosphate.
A. M. Novikova
doaj   +1 more source

Lumbar Spine Chondrocalcinosis [PDF]

open access: yesThe Journal of Rheumatology, 2017
Crystal arthropathy of the lumbar facet joint is a rare but benign differential diagnosis of spondylodiscitis. A 70-year-old woman with a recent sigmoid diverticulitis was examined for a suspicion of infectious spondylodiscitis. She had inflammatory low back pain for a month with low-grade fever and C-reactive protein (CRP) up to 3 mg/dl.
Hélène, Petit   +2 more
openaire   +2 more sources

Chondrocalcinosis and the haemochromatosis-linked HFE C282Y homozygous variant in the UK Biobank

open access: yesEULAR Rheumatology Open
: Objectives: C282Y genetic homozygosity is the main cause of the iron-overload disorder haemochromatosis. Musculoskeletal pain and arthropathy are common in haemochromatosis, but less is known about chondrocalcinosis (cartilage calcification) with the ...
Lucy R Banfield   +4 more
doaj   +1 more source

CPPD—differential diagnostics and differential therapeutic challenges [PDF]

open access: yesExploration of Musculoskeletal Diseases
Calcium pyrophosphate deposition disease (CPPD), characterized by the presence of calcium pyrophosphate crystals in and around joints, poses diagnostic and therapeutic challenges in rheumatology.
Maria L. Voulgari, Herbert Kellner
doaj   +1 more source

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