Results 21 to 30 of about 204,635 (325)

Evolution of Mixed Connective Tissue Disease in 7 Years Old Child: Clinical Case

open access: yesВопросы современной педиатрии, 2020
Background. Mixed connective tissue disease (Sharp syndrome) is the rare chronic autoimmune pathology combining various features of systemic lupus erythematosus, systemic scleroderma, rheumatoid arthritis, dermatomyositis and high antibody titer to ...
Tamara P. Makarova   +6 more
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, 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

Clinical Features of Systemic Sclerosis–Mixed Connective Tissue Disease and Systemic Sclerosis Overlap Syndromes

open access: yesArthritis care & research, 2020
To describe the clinical characteristics and outcomes of systemic sclerosis–mixed connective tissue disease (SSc–MCTD) and SSc overlap syndrome.
J. Fairley   +23 more
semanticscholar   +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

Basophils and IgE contribute to Mixed Connective Tissue Disease development.

open access: yesJournal of Allergy and Clinical Immunology, 2020
BACKGROUND Mixed Connective Tissue Disease (MCTD) is a rare and complex autoimmune disease that presents mixed features with other connective tissue diseases, like systemic lupus erythematosus (SLE), systemic sclerosis and myositis.
Y. Lamri   +12 more
semanticscholar   +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

The role of endothelin-1 in pulmonary arterial hypertension. [PDF]

open access: yes, 2014
Pulmonary arterial hypertension (PAH) is a rare but debilitating disease, which if left untreated rapidly progresses to right ventricular failure and eventually death. In the quest to understand the pathogenesis of this disease differences in the profile,
Chester, AH, Yacoub, MH
core   +1 more source

Mixed connective tissue disease—enigma variations? [PDF]

open access: yesRheumatology, 2016
In 1972, Sharp et al. described a new autoimmune rheumatic disease that they called MCTD, characterized by overlapping features of SSc, SLE, PM/DM, high levels of anti-U1snRNP and low steroid requirements with good prognosis. MCTD was proposed as a distinct disease.
Ciang, NCO, Pereira, N, Isenberg, DA
openaire   +3 more sources

Sudden Onset Blindness in a Patient with Mixed Connective Tissue Disease [PDF]

open access: yes, 2013
Case Presentation A 66-year-old Caucasian female recently diagnosed with mixed connective tissue disease presented with acute onset vision loss in the left eye.
Terry, MSIII, Chris   +2 more
core   +2 more sources

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