Spencer S. Eccles Health Sciences Library, University of Utah
Abstract
Auto-immune optic neuropathy represents a heterogeneous group of conditions, some with recognized systemic autoimmune disease and various autoimmune markers in serologic testing including NMO Abs. Others may present with recurrent visual loss and steroids dependency, but lack any evidence of other systemic inflammatory disease. The aim of this study is to characterize the clinical course of patients with recurrent and/or progressive autoimmune optic neuropathy
