PRMT7 and neurodevelopmental disorder: Biallelic pathogenic variants in PRMT7 (OMIM ∗ 610087) have been associated with a syndromic neurodevelopmental disorder characterized by short stature, brachydactyly, intellectual developmental disability, and seizures, which is currently known as SBIDDS syndrome4, 5, 6, 7, 8, 9 (OMIM 617157).