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.
Jenny Ford has written: 'An investigation into voice quality in eight individuals with osteogenesis imperfecta'
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.