ba0007p223 | (1) | ICCBH2019
Hoseinbeyki Moslem
, Moradifard Shirin
, Mirkhani Fatemeh
, Ehsani Parastoo
, Saghiri Reza
, Karimipoor Morteza
, Alaei Mohammareza
, Ebrahimi-Rad Mina
Objectives: Osteogenesis Imperfecta (OI), is a group of rare, heritable disorder of bone and connective tissue. The pathogenicity of OI arises from the mutations in about 17 different genes, involved in collagen type 1 synthesis, processing, post-translational modification, folding, cross-linking, bone mineralization, and osteoblast differentiation. Based on Sillence classification, there are four types of OI; Type I (mild, non-deforming), Type II (perinatal lethal), Type III ...