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Osteogenesis imperfecta


Osteogenesis imperfecta with blue sclerae: See: Osteogenesis imperfecta type I.
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Osteogenesis imperfecta
Definition:
Osteogenesis imperfecta is a congenital (present from birth) condition of abnormal fragility of the bones.
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Osteogenesis imperfecta (OI), also known as brittle-bone disease, is a genetic (inherited) disorder characterized by bones that break easily without a specific cause. An estimated 20,000 to 50,000 people in the US have this disease.
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AllRefer.com > Health > Diseases & Conditions > Osteogenesis Imperfecta: Diagnosis, Tests, & Signs of Osteogenesis Imperfecta
Osteogenesis Imperfecta
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Osteogenesis imperfecta is a rare form of osteoporosis that is present at birth. Osteogenesis imperfecta causes bones to break for no apparent reason.
Idiopathic juvenile osteoporosis ...
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Osteogenesis imperfecta
Leopard syndrome (multiple lentigines)
Otosclerosis
Robinson type ectodermal dysplasia
Cockayne syndrome
Bjorn pili torti and deafness syndrome
Multiple synostosis syndrome
Hunter syndrome ...
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Osteogenesis imperfecta, a genetic disorder characterized by bones that break easily, often from no apparent cause
Overactive thyroid (hyperthyroidism)
Hyperparathyroidism ...
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Mucopolysaccharidosis (MPS), a series of carbohydrate storage disorders
Osteogenesis imperfecta (brittle bone disease)
Phenylketonuria (PKU), a disease for which newborns are tested
Sickle cell disease. the most common genetic disease in Blacks ...
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