GEMIN5 and Cerebellar atrophy: Recently, biallelic truncating and missense variants in GEMIN5 have been linked to a neurodevelopmental disorder characterized by cerebellar atrophy, developmental and cognitive delay, ataxia, motor dysfunction, and hypotonia named NEDCAM syndrome (neurodevelopmental disorder with cerebellar atrophy and motor dysfunction, OMIM#619333) [13,23,24,25].