This study supports autosomal recessive inheritance of PDS/PG in some families and highlights the potential role of CPAMD8 variants in ocular phenotypes beyond the previously established links with anterior segment dysgenesis [38,39,40] and other glaucoma subtypes (i.e., primary open-angle glaucoma (POAG), primary angle-closure glaucoma (PACG), and congenital glaucoma) [39,41,42,43]. This evidence concerns the gene CPAMD8 and glaucoma.