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International Journal of Rheumatic Diseases, 2021
Patients with juvenile dermatomyositis (JDM) experience muscle weakness, tiredness, and loss of energy, which restrict their abilities in performance of their daily living activities.
R. Elnaggar, Walaa A. Abd El-Nabie
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Patients with juvenile dermatomyositis (JDM) experience muscle weakness, tiredness, and loss of energy, which restrict their abilities in performance of their daily living activities.
R. Elnaggar, Walaa A. Abd El-Nabie
semanticscholar +1 more source
Medical Clinics of North America, 1989
Juvenile dermatomyositis is a chronic disease of childhood that is manifested by severe symmetrical progressive muscle weakness, a characteristic heliotrope colored skin rash which involves the face, and by elevated serum enzymes related to muscle damage.
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Juvenile dermatomyositis is a chronic disease of childhood that is manifested by severe symmetrical progressive muscle weakness, a characteristic heliotrope colored skin rash which involves the face, and by elevated serum enzymes related to muscle damage.
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CYCLOSPORIN IN JUVENILE DERMATOMYOSITIS
The Lancet, 1989Juvenile dermatomyositis in fourteen children who had not responded fully to steroids and other immunosuppressants and who had had chronic active disease for an average of 3 years was successfully treated with cyclosporin. Twelve patients had serious complications of the disease or of previous treatment. The response to cyclosporin included recovery of
J, Heckmatt +8 more
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Retinopathy in juvenile dermatomyositis
The Journal of Pediatrics, 19761. Hughes WT, Feldman S, and Cox F: Infectious diseases in children with cancer, Pediatr Clin North Am 21:583, 1974. 2. Gold E: Serologic and virus-isolation studies on patients with varicella or herpes zoster infections, N Engl J Med 174:181, 1966. 3.
L S, Fruman +3 more
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Juvenile Dermatomyositis and Polymyositis
Clinics in Rheumatic Diseases, 1984Myositis in childhood is characterized by elevated serum levels of muscle-derived enzymes, proximal symmetrical muscle weakness, abnormal EMG and a muscle biopsy which frequently documents an inflammatory process. In the paediatric age group, JDMS is much more common than PM and occurs more frequently among females.
L M, Pachman, M C, Maryjowski
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Hypertrichosis in juvenile dermatomyositis
Journal of the American Academy of Dermatology, 1994A child with juvenile dermatomyositis had extensive, generalized hypertrichosis, a finding not typically associated with dermatomyositis. (J Am Acad Dermatol 1994;31:383-7.)
D N, Pope, R B, Strimling, S B, Mallory
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Juvenile amyopathic dermatomyositis
British Journal of Dermatology, 1997We report a 15-year-old girl with a 10-year-old history of typical skin features of dermatomyositis (DM) without evidence of muscle involvement. Amyopathic dermatomyositis (ADM) is defined by the presence of biopsy confirmed classic cutaneous findings of dermatomyositis in the absence of any clinical or laboratory signs of muscle disease for at least 2
M H, Schmid, R M, Trüeb
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Readability of online patient education materials for juvenile dermatomyositis
Pediatric dermatology, 2021In this study, we sought to analyze the readability of online patient education materials (PEMs) related to juvenile dermatomyositis (JDM). We analyzed the top 100 Google results and using six different readability scores, found 53 PEMs which had an ...
Melissa A. Nickles +4 more
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Calcinosis in juvenile dermatomyositis
Postgraduate Medical Journal, 2010A 61-year-old Caucasian man presented with widespread soft tissue calcinosis. Juvenile dermatomyositis (JDM) had been diagnosed at the age of 12 years, and was treated at the time with high dose corticosteroid. His myositis had been in remission since the age of 16 years, with no new muscle weakness and a normal creatine kinase concentration.
Nicola, Tugnet, David H E, Rees
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Pediatric Clinics of North America, 1986
Myositis in childhood is characterized by elevated serum levels of muscle-derived enzymes, proximal symmetrical muscle weakness, abnormal EMG findings, and a muscle biopsy, which frequently documents an inflammatory process. In the pediatric age group, JDMS, which has characteristic cutaneous involvement in addition to myositis, is much more common ...
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Myositis in childhood is characterized by elevated serum levels of muscle-derived enzymes, proximal symmetrical muscle weakness, abnormal EMG findings, and a muscle biopsy, which frequently documents an inflammatory process. In the pediatric age group, JDMS, which has characteristic cutaneous involvement in addition to myositis, is much more common ...
openaire +3 more sources