ba0007p29 | (1) | ICCBH2019
Zhytnik Lidiia
, Maasalu Katre
, Duy Binh Ho
, Prans Ele
, Reimann Ene
, Koks Sulev
, Martson Aare
Osteogenesis Imperfecta (OI) is a rare congenital disorder of bone fragility. Majority of OI cases are caused by loss of function or missense pathogenic variants in the COL1A1/2 genes. In addition to fractures, patients suffer from different, mainly long bone, skeletal deformities. OI patients might develop chest deformities (pectus carinatum (PC) or excavatum (PE)) of different severity, which can tend to formation of cardiopulmonary complications. The main aim of current stu...