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Genetic and Metabolic :
Osteogenesis Imperfecta

OI, sometimes known as Brittle Bone Disease or "Lobstein syndrome", is a genetic bone disorder. It is usually because of deficiency in the Type 1 collagen that results in deficient connective tissue.

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New Model of Understanding Osteogenesis Imperfecta
Osteogenesis imperfecta (OI) is the most common genetic form of the brittle bone disease characterized by short stature, skeletal deformities, low bon.....
Urban Population at High Risk for Brittle Bones
People living in the city are at high risk of suffering from brittle bones which can cause fractures even with simple acts like bending over or coughi.....
Understanding the Functional Consequences of Osteogenesis Imperfecta Type IV
Osteogenesis Imperfecta (OI) is caused by genetic defects that affect the body’s ability to make strong bones, it is a heritable disorder characterize.....
HIV-Infected Men Suffer from Brittle Bones More Than Women
Men infected with human immunodeficiency virus (HIV) are at greater risk of suffering from brittle and fragile bones than women, claims a new research.....
World’s First Stem Cell Therapy in the Womb Focuses On Treating Brittle Bone Disease
One in every 25,000 births are affected by a brittle bone disease called osteogenesis imperfecta. It is caused by errors in the developing baby's DNA,.....


About Osteogenesis Imperfecta
Encyclopedia section of Medindia gives general info about Osteogenesis Imperfecta.. Read More



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