Snijders Blok–Campeau syndrome (SNIBCPS) (MIM #618205) is a notably infrequent autosomal dominant disease, first described by Snijders Blok et al. in 2018 [1] and caused by pathogenic and likely pathogenic variants in the Chromodomain Helicase DNA Binding Protein 3 (CHD3) gene. Here, CHD3 is linked to Snijders Blok-Campeau syndrome.