The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype

Abstract Sporadic inclusion body myositis (sIBM) usually occurs as an isolated condition, but it may occur in association with another autoimmune disorder such as Sjögren's syndrome. We reviewed sIBM cases with Sjögren's syndrome (sIBM/SS) from the Perth Inflammatory Myopathies Database to...

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Veröffentlicht in:	Clinical neurology and neurosurgery 2011-09, Vol.113 (7), p.559-563
Hauptverfasser:	Rojana-udomsart, A, Needham, M, Luo, Y.B, Fabian, V, Walters, S, Zilko, P.J, Mastaglia, F.L
Format:	Artikel
Sprache:	eng
Schlagworte:	8.1 MHC ancestral haplotype Age of Onset Autoimmune diseases Biological and medical sciences Creatine Kinase - metabolism Cytokines Disease Female Females Genes, MHC Class I - genetics Genotype Haplotypes Heterozygote HLA Antigens - genetics HLA-DR3 HLA-DR3 Antigen - genetics HLA-DRB10301 Humans Hypothyroidism Medical sciences Middle Aged Muscle Strength - physiology Muscle, Skeletal - pathology Muscular Diseases - genetics Muscular Diseases - pathology Muscular system Myositis, Inclusion Body - complications Myositis, Inclusion Body - genetics Myositis, Inclusion Body - pathology Necrosis Neurology Neurosurgery Sjogren's Syndrome - complications Sjogren's Syndrome - genetics Sjogren's Syndrome - pathology Sjögren's syndrome Sporadic inclusion body myositis Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
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