ENAMEL ALTERATIONS IN SEROTONIN 2B RECEPTOR KNOCKOUT TWICE
The role of the serotonin 2B receptor (5-HT2BR) in enamel formation and mineralization was explored in adult 5-HT2BR knockout (KO) mice compared with wild-type (WT) mice...
A NEW OSTEOGENESIS IMPERFECTA WITH IMPROVEMENT OVER TIME MAPS TO 11Q
Osteogenesis imperfecta (OI) is basically divided into four clinical types, I-IV. Type IV clearly represents a heterogeneous group of disorders. Here we describe two QI patients...
PRENATAL CORTICAL HYPEROSTOSIS WITH COL1A1 GENE MUTATION
Infantile cortical hyperostosis (Caffey disease) is benign and self-limiting when it presents near of after birth but it is usually lethal when it presents earlier. We present the clinical...
INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY DISEASE) : A REVIEW
Infantile cortical hyperostosis is usually a self-limiting inflammatory disease that begins in early infancy. It is characterized by unusual irritability, soft tissue swelling and...
ANIMAL MODELS OF OSTEOGENESIS IMPERFECTA AND RELATED SYNDROMES
Osteogenesis imperfecta (OI) is a genetic disorder of increased bone fragility and low bone mass. Severity varies widely, ranging from intrauterine fractures and perinatal lethality...
ÉCHEC AUX ÉCHECS - LE PATIENT ORTHODONTIQUE : ALÉAS ET SOLUTIONS
Confronté à des demandes grandissantes de ses patients, et à des évolutions technologiques multiples, l'omnipraticien ne peut pas toujours assurer des soins conformes aux...
