Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations|
Discussed are defects in four key physiologic processes in bone/tooth formation that serve as models for the understanding of other diseases in the skeleton and dental-oral-craniofacial complex: progenitor cell differentiation (fibrous dysplasia), extracellular matrix production (osteogenesis imperfecta), mineralization (familial tumoral calcinosis/hyperostosis hyperphosphatemia syndrome, hypophosphatemic rickets, and hypophosphatasia), and bone resorption (Gorham-Stout disease). [J Dent Res] Abstract |
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