Serum antibodies directed against myelin oligodendrocyte glycoprotein (MOG) are found in
patients with acquired CNS demyelinating syndromes that are distinct from multiple sclerosis …

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is the
most recently defined inflammatory demyelinating disease of the central nervous system …

Accurate diagnosis of multiple sclerosis requires careful attention to its differential diagnosis—
many disorders can mimic the clinical manifestations and paraclinical findings of this …

Neuromyelitis optica (NMO; also known as Devic syndrome) is a clinical syndrome
characterized by attacks of acute optic neuritis and transverse myelitis. In most patients …

There is no consensus regarding the classification of optic neuritis, and precise diagnostic
criteria are not available. This reality means that the diagnosis of disorders that have optic …

Autoimmunity plays a significant role in the pathogenesis of demyelination. Multiple
sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD) and myelin …

Optic neuritis (ON) is the most common cause of subacute optic neuropathy in young adults.
Although most cases of optic neuritis (ON) are classified as typical, meaning idiopathic or …

Neuromyelitis optica spectrum disorders (NMOSDs) and myelin oligodendrocyte
glycoprotein-antibody-associated disease (MOGAD) are autoimmune inflammatory …

PURPOSE OF REVIEW Anti–myelin oligodendrocyte glycoprotein (MOG) autoantibodies
have become a recognized cause of a pathophysiologically distinct group of central nervous …

Optic neuritis (ON) is one of the most frequently seen neuro-ophthalmic causes of vision loss
worldwide. Typical ON is often idiopathic or seen in patients with multiple sclerosis, which is …