LARP7 and microcephalic primordial dwarfism, Alazami type: Alazami syndrome (MIM 615071) is an ultra-rare autosomal recessive syndromal form of NDD, described for the first time in 2012 in an inbred Saudi Arabian family with a novel form of primordial dwarfism, due to a homozygous variant in LARP7 (OMIM 612026) gene [4].