Alazami Syndrome (ALAZS)

Alazami Syndrome, also known as microcephalic primordial dwarfism, alazami type, is related to persistent hyperplastic primary vitreous, autosomal recessive and amed syndrome, digenic. An important gene associated with Alazami Syndrome is LARP7 (La Ribonucleoprotein 7, Transcriptional Regulator). Affiliated tissues include eye and testis, and related phenotypes are widely spaced teeth and intellectual disability, severe