HNRNPH1 and Neurodevelopmental delay: Despite a small number of HNRNPH1-mutated patients that have been clinically evaluated so far (seven plus a fetus), the high sequence homology (96%) of hnRNPH1 and hnRNPH2 has immediately raised the cross-comparison of unique and overlapping phenotypic features of this new NDD with the previously described H2-related syndromic ID (Bain et al., 2016, 2021).