Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8736363 | Autoimmunity Reviews | 2018 | 4 Pages |
Abstract
Approximately 10% of cSLE had symptomatic PA at diagnosis, particularly endocrine autoimmune disorders and antiphospholipid syndrome. Lupus was characterized by a mild disease onset and MAS was infrequently evidenced. Further studies are necessary to determine if this subgroup of cSLE patients have a distinct genetic background with a less severe disease and a better long-term outcome.
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Authors
Debora N. Setoue, Ana C. Pitta, Fernanda J. Fiorot, Mariana M. Nastri, Glaucia V. Novak, Beatriz C. Molinari, Juliana C. Oliveira, Natali W. Gormezano, Ana P. Sakamoto, Maria T. Terreri, Rosa M. Pereira, Claudia Saad-Magalhães, Adriana M. Sallum,