Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9369644 | Archives de Pédiatrie | 2005 | 8 Pages |
Abstract
Conclusion. - ES was a severe, life-threatening disease, requiring aggressive immunosuppressive therapy in as many as half the patients. Our forthcoming study aims to (i) describe homogeneously-studied and prospectively-analysed cohort of childhood ES, (ii) separate ES from specific immune deficiency (especially fas gene mutations), generalised autoimmune/inflammatory disorders and genetic diseases, (iii) identify well-defined ES subsets, (iv) establish prognostic factors and optimal treatment within these subsets.
Keywords
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Authors
P. Blouin, A. Auvrignon, A. Pagnier, I. Thuret, G. Antoni, B. Bader-Meunier, F. Le Deist, P. Chastagner, N. Aladjidi, I. Pellier, Y. Bertrand, C. Behar, J. Landmann-Parker, G. Leverger, Y. Perel,