Al-Gazali Syndrome (ALGAZ)

Al-Gazali Syndrome, also known as algaz, is related to clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly and ehlers-danlos syndrome, spondylodysplastic type, 2. An important gene associated with Al-Gazali Syndrome is B3GALT6 (Beta-1,3-Galactosyltransferase 6). Affiliated tissues include eye, and related phenotypes are failure to thrive and osteopenia