Osteogenesis Imperfecta Research Paper

Osteogenesis imperfecta (OI) is a genetic disorder that affects the skeletal system. The disorder affects the bones, it makes them fragile and easy to break. OI has many different types; type I one being the most common and mildest, and type II is the most severe. The first case of OI was found in a partially mummified infant's skeleton found from ancient Egypt. In 1835, Jean Lobstein made the term for osteogenesis imperfecta and was the first to correctly understand the causes of the disorder. OI can be known as Lobstein disease, brittle-bone disease, blue-sclera syndrome, and fragile-bone disease.
There are many different types of OI, depending on the type there are various different symptoms. The most common symptoms are short stature,