Abstract
Mixed connective tissue disease (MCTD) was described in 1972 by Sharp et al (1) as a syndrome of overlapping features of systemic lupus erythematosus (SLE), progressive systemic sclerosis (PSS), and myositis. The serum of MCTD patients characteristically contained high titers of antibody to nuclear ribonucleoprotein (RNP) (2,3). While the initial report stressed the paucity of renal involvement in MCTD, subsequent studies of adults (4–13) and children (14–18) noted a higher prevalence of nephropathy (10–50%).
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© 1989 Plenum Press, New York
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Akmal, M. (1989). Mixed Connective Tissue Disease and Renal Disease. In: Amerio, A., Coratelli, P., Campese, V.M., Massry, S.G. (eds) Drugs, Systemic Diseases, and the Kidney. Advances in Experimental Medicine and Biology, vol 252. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8953-8_5
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DOI: https://doi.org/10.1007/978-1-4684-8953-8_5
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