Mutations in RPL10 (Gene ID: 6134) have been associated with the onset of autism [125], intellectual disability associated with cerebellar hypoplasia and spondyloepimetaphyseal dysplasia [126], microcephaly [127], and mutations in RPS23 (Gene ID: 6228) associated with microcephaly and hearing loss combined with growth deficits and dysmorphic features [128]. Here, RPS23 is linked to microcephaly.