Pediatric insufficiency
Osteogenesis imperfecta is also called brittle bone disease. Presented as a systemic connective tissue abnormality. It is characterized by multiple fractures, blue sclera, progressive deafness, tooth changes, joint relaxation and skin abnormalities. Genetics is mostly autosomal dominant, and in some cases it is recessive. Intergenerational cases have also been reported.
The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.