I can honestly say that it does not stop me at all. I still skateboard and snowboard and haven't hurt myself doing either. I live like any other 16 year old boy, my eyes are just prettier.
Osteogenesis imperfecta is typically inherited in an autosomal dominant pattern, meaning one copy of the mutated gene is enough to cause the condition. However, in some cases, it can be inherited in an autosomal recessive pattern if both parents are carriers of the mutated gene.
Osteogenesis imperfecta primarily affects the bones in the body, leading to brittle bones that are prone to fractures. It can also affect other connective tissues such as ligaments and tendons. Symptoms can vary widely depending on the type and severity of the condition.
Osteoprogenitor cells, also known as mesenchymal stem cells, are the first type of cell to appear during osteogenesis. These cells have the potential to differentiate into osteoblasts, which are responsible for bone formation.
The symptoms described—knobby rib cage, enlarged forehead, and bent lower limbs—are indicative of a condition known as osteogenesis imperfecta (OI), commonly referred to as "brittle bone disease." This genetic disorder affects collagen production, leading to fragile bones, skeletal deformities, and distinctive facial features. The combination of these symptoms suggests a possible type of OI, which requires further clinical evaluation for confirmation and management options.
The term "limiting" is used to describe the reactant that is completely consumed in a chemical reaction, thus limiting the amount of product that can be formed. It determines the maximum amount of product that can be produced based on its stoichiometry and quantity.
USA
Lack of calcium can lead to Osteogenesis Imperfecta
Type I Osteogenesis Imperfecta is the most common and mildest type of this disease. In this type the Scleras (whites of the eyes) usually have a blue, purple, or gray tint.
premature infants(as normal finding),rickets,osteogenesis imperfecta
Yes, because it is a genetic disease you inherit from your parents.
Osteoporosis occurs later in life and leads to weakening and fractures of the bones. Osteogenesis imperfecta is a congenital defect which causes fractures to occur from the slightest bump or touch in a child.
Osteogenesis imperfecta, also known as brittle bone disease, was first described by British surgeon John F. Clarke in 1695. He observed patients with fragile bones that easily fractured, leading to the recognition of this genetic disorder.
Osteogenesis imperfecta is a genetic disorder that causes brittleness of one bones. This can cause ones bones to break easily and even for no apparent reason. Also, it can lead to abnormally large amounts of repair tissue at the site of fractures.
osteogenesis imperfecta - brittle bone disease
Osteogenesis imperfecta means poor development of bones.
"some people may only grow to be three feet tall"sourcehttp://www.orthop.washington.edu/?q=patient-care/articles/arthritis/osteogenesis-imperfecta.html
Jenny Ford has written: 'An investigation into voice quality in eight individuals with osteogenesis imperfecta'