Three M Syndrome 2 (3M2)

Three M Syndrome 2, also known as 3m syndrome 2, is related to renal hypoplasia and three m syndrome 1. An important gene associated with Three M Syndrome 2 is OBSL1 (Obscurin Like Cytoskeletal Adaptor 1). Affiliated tissues include tongue and bone, and related phenotypes are frontal bossing and delayed skeletal maturation