Orthopedic Conditions
Osteogensis Imperfecta is a genetic bone disease characterized by bones which are weaker and that break easily. There are eight types of OI, and which type the child has dictates the severity of the symptoms. Children may also may have a blue tint to the whites of their eyes and hearing loss due to weak bones in the inner ear. Children with OI generally have poor dental structure and loose joints. More severe forms of OI may include bowed legs and arms, kyphosis (hunched back) and/or scoliosis.
There are many families that have adopted a child with Osteogenesis Imperfecta, club foot, or other orthopedic differences. Please use our website to read family adoption stories, view children waiting to be adopted, and learn more about this and other medical conditions experienced by children living in institutions and orphanages.
The prognosis for this condition varies greatly depending on the severity of symptoms. For children with mild symptoms, life expectancy is not impacted. For children with more severe symptoms, their life expectancy may be shorter. Most people with OI however, lead very successful lives.
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