CLINICAL CASE OF RARE TYPE V OSTEOGENESIS IMPERFECTA

• Main Authors: G. T. Yakhyayeva (Author), T. V. Margieva (Author), L. S. Namazova-Baranova (Author), K. V. Savostyanov (Author), A. A. Pushkov (Author), N. V. Zhurkova (Author), K. V. Zherdev (Author), N. D. Vashakmadze (Author), A. K. Gevorkyan (Author)
• Format: Book
• Published: Union of pediatricians of Russia, 2015-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Osteogenesis imperfecta, also known as the brittle bone disease, is a clinically heterogenic hereditary connective tissue disease characterized by brittle bones and high risk of skeletal bone fractures. Other observable symptoms, such as deformities of limb and spinal bones, blue sclerae, dentinogen...