Seminar I🤩 Osteogenesis Imperfecta

The first week that we shared information about Osteogenesis Imperfecta in public was successful!🤩

We organized a seminar which contained more than fifty students and listened what public knew about Osteogenesis Imperfecta (OI)

About Osteogenesis Imperfecta (OI)
Ol is a group of genetic disorders that impact bone metabolism. Approximately 85% to 90% of OI cases are caused by mutations in the COL1A1 or COL1A2 genes, leading to bone resorption and inadequate production of new bone. Patients with OI can experience brittle bones, fractures, bone deformities, pain, short stature, and decreased mobility.

Osteogenesis imperfecta (OI) is an inherited (genetic) bone disorder that is present at birth. It is also known as brittle bone disease. A child born with OI may have soft bones that break (fracture) easily, bones that are not formed normally, and other problems. Signs and symptoms may range from mild to severe.

Our members wish to help those Osteogenesis Imperfecta children and make them enjoy the beautiful life❤️