Unusual Clinical and Imaging Features of MOGAD in Two Pediatric Patients (P7-6.017)

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) has emerged as a significant etiology of acquired CNS demyelinating syndromes. While the clinical features are well established in adults, the presentation can be confusing and require extensive investigations in the pediatric population. We present two cases diagnosed with MOGAD, highlighting their unusual clinical and imaging manifestations.