B8, DR5, DR3 (tineri); HLA-A3, D7, DRW2 (varsnici) Congenitale (defecte genetice) Clinic Debut Posibil favorizat de factori infecioi, toxici, traumatici, endocrini Zile-sptmni
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ACh receptori Vrsta medie de debut: a 3a decad (20-40 ani): femei>brbai A sasea/saptea decada: barbati = femei Forme Sporadic (autoimun eventual susceptibilitate genetic) HLA-A1
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