SLC13A5 and amelogenesis imperfecta: Autosomal recessive variants of the SLC13A5 gene (MIM*608305) have been reported to cause developmental and epileptic encephalopathy 25 with amelogenesis imperfecta (DEE25, MIM #615905) in early infancy (Matricardi et al., 2020; Milosavljevic et al., 2022).