Osteogenesis Imperfecta in Children
Osteogenesis imperfecta (OI) is an inherited (genetic) bone disorder that is present at birth. It is also known as brittle bone disease. A child born with OI may have soft bones that break (fracture) easily, bones that are not formed normally, and other problems. Signs and symptoms may range from mild to severe.
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Medical Genetics
The Medical Genetics Program at Mass General for Children specializes in the evaluation and care of patients of all ages who may have health problems with a hereditary, genetic, or metabolic basis.
Pediatric Bone and Mineral Metabolism Disorders Clinic
Our clinic specializes in the treatment of low bone density, osteoporosis, vitamin D deficiency, rickets and osteomalacia and other disorders affecting bone health and mineral metabolism in infants, children and young adults.
Pediatric Endocrine Program and Diabetes Center
The Division of Pediatric Endocrinology and Diabetes Center at Mass General for Children is an international referral center for the management of pediatric diabetes and endocrine disorders in children and adolescents.
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