Results 41 to 50 of about 378,540 (249)

The von Willebrand Factor Antigen Reflects the Juvenile Dermatomyositis Disease Activity Score

open access: yesBiomedicines, 2023
Objective: This study determined if an accessible, serologic indicator of vascular disease activity, the von Willebrand factor antigen (vWF:Ag), was useful to assess disease activity in children with juvenile dermatomyositis (JDM), a rare disease, but ...
Ellie Gibbs   +4 more
semanticscholar   +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

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

Juvenile dermatomyositis. Where are we now?

open access: yesClinical and Experimental Rheumatology, 2022
Juvenile onset idiopathic inflammatory myopathy (IIM) has many similarities and distinct differences from adult-onset disease. This review will focus on recent developments in understanding and treatment of juvenile dermatomyositis (JDM), the most common
L. McCann   +3 more
semanticscholar   +1 more source

Erythroderma as a presenting sign of juvenile overlap syndrome

open access: yesIndian Journal of Paediatric Dermatology, 2023
Juvenile dermatomyositis (JDM), which is rarely presented with erythroderma, and juvenile morphea are both autoimmune connective tissue diseases. We report a 14-year-old male child with resistant generalized erythroderma and mild proximal muscle weakness
Sarah Hamdy Soliman   +5 more
doaj   +1 more source

A rare case of suspected lupus erythematosus panniculitis as the presenting skin feature of juvenile dermatomyositis: A case report

open access: yesSAGE Open Medical Case Reports, 2022
Juvenile dermatomyositis is a rare autoimmune myopathy of childhood, associated with systemic vasculopathy, primarily affecting the capillaries. Panniculitis is seen histologically in about 10% of patients with dermatomyositis; however, its clinical ...
Dylan C Ginter   +5 more
doaj   +1 more source

Role of CD14+ monocyte-derived oxidised mitochondrial DNA in the inflammatory interferon type 1 signature in juvenile dermatomyositis

open access: yesAnnals of the Rheumatic Diseases, 2022
Objectives To define the host mechanisms contributing to the pathological interferon (IFN) type 1 signature in Juvenile dermatomyositis (JDM). Methods RNA-sequencing was performed on CD4+, CD8+, CD14+ and CD19+ cells sorted from pretreatment and on ...
M. Wilkinson   +14 more
semanticscholar   +1 more source

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   +1 more source

JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study.

open access: yesRheumatology, 2021
OBJECTIVE To evaluate the efficacy and safety of JAK inhibitors (JAKi) in juvenile dermatomyositis (JDM). METHODS We conducted a single-center retrospective study of patients with JDM treated by JAKi with a follow-up of at least 6 months. Proportion of
Tom Le Voyer   +14 more
semanticscholar   +1 more source

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