MOG-Associated Disease: Clinical and Paraclinical Study of a Tunisian Pediatric Series

Myelin oligodendrocyte glycoprotein encephalomyelitis-associated disease (MOGAD) is a primitive, acquired and immune mediated demyelinating syndrome of the central nervous system (CNS). It is characterized by attacks of immune-mediated demyelination predominantly targeting the optic nerves, brain, and spinal cord. In Tunisia, there was rare published series of MOGAD.