| Literature DB >> 27032791 |
Roberta A Berard1,2, Ronald M Laxer3,4.
Abstract
Pediatric-onset mixed connective tissue disease is among the rare disease entities in pediatric rheumatology and includes features of arthritis, polymyositis/dermatomyositis, systemic lupus erythematosus, and systemic sclerosis. Accurate recognition and diagnosis of the disease is paramount to prevent long-term morbidity. Advances in the genetic and immunologic understanding of the factors involved in the etiopathogenesis provide an opportunity for improvements in prognostication and targeted therapy. The development of a multinational cohort of patients with mixed connective tissue disease would be invaluable to provide more updated data regarding the clinical presentation, to develop a standardized treatment approach, disease activity and outcome tools, and to provide data on long-term outcomes and comorbidities.Entities:
Keywords: Etiopathogenesis; Mixed connective tissue disease; Outcome; Pediatric; Treatment
Mesh:
Substances:
Year: 2016 PMID: 27032791 DOI: 10.1007/s11926-016-0576-x
Source DB: PubMed Journal: Curr Rheumatol Rep ISSN: 1523-3774 Impact factor: 4.592