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Osteogenesis imperfecta congenita which is apparent at birth and osteogenesis imperfecta tarda which manifests itself usually in. Traditionally the disease has been recognized in two forms.

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One per million people.

. Mandibuloacral dysplasia pyknodysostosis osteogenesis imperfecta Hajdu-Cheney syndrome. Osteogenesis imperfecta or brittle bone disease is a group of hereditary connective tissue disorders characterized by unusual bone fragility and tendency to fracture. The collarbones are typically either poorly developed or.

Cleidocranial dysostosis CCD also called cleidocranial dysplasia is a birth defect that mostly affects the bones and teeth.

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Fig 1 The Bmj

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Developmental Charts For The Body Mass Of Children With Type I Download Scientific Diagram

Developmental Charts For The Body Height Of Children With Type I Download Scientific Diagram

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References In Skeletal Effects And Functional Outcome With Olpadronate In Children With Osteogenesis Imperfecta A 2 Year Randomised Placebo Controlled Study The Lancet