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See Latest ArticlesA systematic review of juvenile-onset clinically amyopathic dermatomyositis
British Journal of Dermatology, 09/14/07
Gerami, P., et al. - Conclusions: This review suggests a good prognosis for children with clinically amyopathic DM. A minority of patients with negative muscle enzymes had positive ancillary testing for myositis, and these patients rarely developed muscle weakness. Predictive factors for progression to classical DM were not identified. Symptomatic treatment of cutaneous involvement and close clinical monitoring may be an alternative to aggressive immunosuppression
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