Results 21 to 30 of about 63,561 (137)

Mixed connective tissue disease: presenting as trigeminal neuralgia

open access: yesThe Egyptian Journal of Internal Medicine, 2022
Connective tissue diseases (autoimmune rheumatic diseases) are a group of disorders of unknown etiology. The term mixed connective tissue (MCTD) is used when two or more autoimmune diseases occur in the same individual simultaneously, for example ...
Gladwin Jeemon, T. H. Neha
doaj   +1 more source

Capillaroscopy as a diagnostic tool in the diagnosis of mixed connective tissue disease (MCTD): a case report

open access: yesBMC Rheumatology, 2021
Background The concept of mixed connective tissue disease (MCTD) as a unique connective tissue disease has endured for half a century. Disease onset can be in adulthood (MCTD) or of juvenile onset (jMCTD) and is characterized by overlapping features of ...
Mislav Radić, Rebecca S. Overbury
doaj   +1 more source

Mixed connective tissue disease

open access: yesСовременная ревматология, 2019
Mixed connective tissue disease (MCTD), also known as Sharp's syndrome, is a rare systemic connective tissue disorder that characterized by a combination of some features of systemic lupus erythematosus, systemic sclerosis, rheumatoid arthritis ...
R. U. Shayakhmetova, L. P. Ananyeva
doaj   +1 more source

Severe sensory ganglionopathy as a manifestation of mixed connective tissue disease [PDF]

open access: yesRomanian Journal of Neurology, 2022
Sensory ganglionopathies (SG) are a rare but distinct clinical subgroup of peripheral neuropathies characterized by damage to dorsal root ganglia. Typical manifestations include early gait and limb ataxia, widespread diminished or absent deep tendon ...
Adina Stan   +4 more
doaj   +1 more source

Mixed connective tissue disease, undifferentiated connective tissue disease and overlap syndromes

open access: yesAlʹmanah Kliničeskoj Mediciny, 2019
Systemic lupus erythematosus, systemic sclerosis, inflammatory myopathy and rheumatoid arthritis are systemic connective tissue disorders which are characterized by heterogeneous clinical symptoms and variable course. To date, updated diagnostic criteria
R. T. Alekperov
doaj   +1 more source

Interstitial lung disease in mixed connective tissue disease

open access: yesIndonesian Journal of Rheumatology, 2017
Interstitial lung diseases (ILD) are known as a debilitating pulmonary complications that may be occured in almost all systemic connective tissue diseases (CTD), including mixed connective tissue disease (MCTD).
Marshell Tendean   +2 more
doaj   +1 more source

Breast involvement in mixed connective tissue disease

open access: yesRadiology Case Reports, 2019
To date, mammographic involvement in mixed connective tissue disease has not been described in the literature to the authors’ knowledge. In addition, only 2 case reports have described panniculitis in mixed connective tissue disease. We present a patient
Ross Varma, MD   +2 more
doaj   +1 more source

Mixed Connective Tissue Disease with Severe Axonal Polyneuropathy: A Case Report. [PDF]

open access: yesOman Med J, 2022
Mixed connective tissue disease (MCTD) is a unique disorder characterized by the presence of a high titer of anti-U1 ribonucloprotein antibody with overlapping features of various connective tissue disorders including systemic lupus erythematosus ...
Al Lawati T, Hassan B.
europepmc   +2 more sources

Elevated IgG Antibody to Aluminum Bound to Human Serum Albumin in Patients with Crohn’s, Celiac and Alzheimer’s Disease

open access: yesToxics, 2021
Aluminum is in our water and food, and is used as an adjuvant in vaccines. About 40% of the ingested dose accumulates within the intestinal mucosa, making the gut the main target of inflammation and autoimmunity; about 1% accumulates in the skeletal ...
Aristo Vojdani
doaj   +1 more source

Association study between immune-related miRNAs and mixed connective tissue disease

open access: yesArthritis Research & Therapy, 2021
Background Mixed connective tissue disease (MCTD) is a rare condition that is distinguished by the presence of specific U1-RNP antibodies. Information about its etiopathology and diagnostics is still unclear.
Barbara Stypińska   +4 more
doaj   +1 more source

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