Results 11 to 20 of about 6,997 (186)

A Cause of High Creatine Kinase: A Case of Juvenile Dermatomyositis

open access: yesHaseki Tıp Bülteni, 2014
Although juvenile dermatomyositis is rare, it is the most common idiopathic nonsupurrative inflammatory myositis in childhood. Skin lesions, proximal muscle weakness, elevated levels of muscle enzymes, electromyography, and muscle biopsy findings are ...
İsmail Yıldız   +7 more
doaj   +2 more sources

Calcinosis in juvenile dermatomyositis: Updates on pathogenesis and treatment

open access: yesFrontiers in Medicine, 2023
Calcinosis, or the deposition of insoluble calcium salts in the skin, subcutaneous tissue, fascia, tendons, and muscles, is a feared complication of juvenile dermatomyositis.
Caitlan S. Pinotti   +4 more
doaj   +3 more sources

Being on the juvenile dermatomyositis rollercoaster: a qualitative study [PDF]

open access: yesPediatric Rheumatology Online Journal, 2019
Background Juvenile Dermatomyositis is a rare, potentially life-threatening condition with no known cure. There is no published literature capturing how children and young people feel about their condition, from their perspective.
Polly Livermore   +5 more
doaj   +3 more sources

CORRELATIONS BETWEEN NAILFOLD CAPILLAROSCOPY FINDINGS AND DISTINCT CLINICAL FORMS OF JUVENILE DERMATOMYOSITIS [PDF]

open access: yesRomanian Journal of Rheumatology, 2019
Juvenile dermatomyositis is the most common idiopathic inflammatory myopathy in childhood. Nailfold capillaroscopy plays an important role in its assessment, being useful for diagnosis and follow-up.
Sigrid Covaci   +2 more
doaj   +2 more sources

Case of a fatal lung disease in a child with juvenile dermatomyositis

open access: yesZdorovʹe Rebenka, 2017
The article presents a case of a fatal lung disease in a child with juvenile dermatomyositis. Juvenile dermatomyositis is a serious disease with an unpredictable course, and lung damage in juvenile dermatomyositis is one of the most severe manifestations
O.A. Oshlianska   +5 more
doaj   +2 more sources

Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis

open access: yesClinics, 2012
OBJECTIVE: To analyze major histocompatibility complex expression in the muscle fibers of juvenile and adult dermatomyositis. METHOD: In total, 28 untreated adult dermatomyositis patients, 28 juvenile dermatomyositis patients (Bohan and Peter's criteria)
Samuel Katsuyuki Shinjo   +3 more
doaj   +2 more sources

A fatal interstitial lung disease in an anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody negative patient with juvenile dermatomyositis

open access: yesThe Turkish Journal of Pediatrics, 2021
Background. Juvenile dermatomyositis associated interstitial lung disease, rarely seen in pediatric age groups, has adverse effects on survival.
Osman Yeşilbaş   +9 more
doaj   +1 more source

Juvenile dermatomyositis and nephrotic syndrome: A case report and a mini literature review

open access: yesFrontiers in Pediatrics, 2023
BackgroundRenal involvement is rarely reported in juvenile dermatomyositis and may be caused by the toxic effects of myoglobinuria or an autoimmune reaction. We report a case of dermatomyositis and nephrotic syndrome in a child to explore the association
Weiran Zhou   +4 more
doaj   +1 more source

An 8-year-old-girl with juvenile dermatomyositis and autoimmune thyroiditis in Tanzania: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Juvenile dermatomyositis is an inflammatory disease of muscles, skin, and blood vessels of unknown cause affecting all age and ethnic groups, with a reported incidence of 1.9–4.1 per million.
Fatima Mussa   +2 more
doaj   +1 more source

Clinical and autoantibody phenotypes of juvenile dermatomyositis

open access: yes, 2022
Juvenile dermatomyositis (JDM) is a heterogeneous autoimmune inflammatory myositis with symmetrical proximal muscle weakness and a characteristic rash. Juvenile dermatomyositis is characterized by variable presentation and phenotypes.
Iryna Yuryk   +5 more
core   +1 more source

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