About Osteogenesis Imperfecta
Osteogenesis imperfecta is a serious disease of the bone with no known cause. As the name indicates, the disease affects the bones during their formation in vivo and renders them brittle. This condition occurs in two forms—one is present at birth and the other manifests later in childhood. Almost all infants with the former type of Osteogenesis imperfecta are stillborn or die shortly after birth.
Latest Publication and Research on Osteogenesis ImperfectaSite-Specific Quantitative Analysis of Overglycosylation of Collagen in Osteogenesis Imperfecta Using Hydrazide Chemistry and SILAC. - Published by PubMed
Osteogenesis Imperfecta/Lobstein Syndrome associated with Dentinogenesis Imperfecta. - Published by PubMed
Thoracolumbar Junction Syndrome Causing Pain around Posterior Iliac Crest: A Case Report. - Published by PubMed
Traumatic cardiac arrest in a patient with osteogenesis imperfecta. - Published by PubMed
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome. - Published by PubMed