Typical optic neuritis (ON) presents with acute, unilateral, onset of variable visual acuity/visual field loss, retrobulbar pain (worse with eye movement), loss of color vison, a relative afferent …

Bilateral involvement, disc swelling clinically and radiologically, and longitudinally extensive optic nerve hyperintensity with associated optic perineuritis on MRI are key characteristics that can …

Several distinct clinical phenotypes have been identified in MOGAD including optic neuritis, myelitis, brainstem syndrome, acute dissemination encephalomyelitis, and cortical encephalitis.

2024年11月15日 · Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory disorder of the central nervous system characterized by attacks of immune …

Two novel glial autoantibodies discovered in the past 15 years enable recognition of patient subsets with antigen-specific central nervous system (CNS) inflammatory demyelinating …

Identification of optic neuritis characteristic in MS, MOG-AD and NMOSD is important as the visual prognosis and treatment approach varies. We present three cases of MOG-ON with …

Manifestations of MOG-IgG-positive optic neuritis are diverse. Despite recurrent attacks with severe vision loss, the majority of patients have significant recovery and retain functional …

Read detailed information about the signs and symptoms of MOGAD (MOG antibody disease) such as vision loss, paralysis, loss of sensation, and more.

2024年5月24日 · Bilateral involvement, disc swelling clinically and radiologically, and longitudinally extensive optic nerve hyperintensity with associated optic perineuritis on MRI are …

2024年4月19日 · In eyes with first MOG-associated ON episodes, milder enhancement in the orbital optic nerve was associated with poorer VA and visual field recovery. Prospective and …