ba0007p106 | (1) | ICCBH2019
Khan Sobiah
, Yonko Elizabeth
, Carter Erin
, Sandhaus Robert
, Raggio Cathleen
Objectives: Osteogenesis imperfecta (OI) is a group of rare genetic disorders characterized by osteoporosis, predisposition to fracture, and scoliosis. Recently, however, there has been increased focus on pulmonary insufficiency, as it is the leading cause of mortality in individuals with OI. The primary objective of this study is to determine if reduced pulmonary function in individuals with OI is intrinsic to the underlying connective tissue disorder. Another goal of this st...