Article
Osteogenesis imperfecta--clinical and molecular diversity.
European cells & materials - 30 Jun 2003
Roughley P J, Rauch F, Glorieux F H
Abstract excerpt
Osteogenesis imperfecta is a heritable disorder of bone formation resulting in low bone mass and a propensity to fracture. It exhibits a broad range of clinical severity, ranging from multiple fracturing in utero and perinatal death to normal adult stature and a low fracture incidence. The disorder is currently classified into seven types based on differences in clinical presentation and bone architecture....
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
