Nouveautés dans l'ostéogenèse imparfaite: de la recherche à la prise en charge multidisciplinaire [News in osteogenesis imperfecta: from research to clinical management]

Osteogenesis imperfecta (OI) is a rare genetic disease. Today we are able to propose an adapted and efficient management to the patients with this rare disorder (and their families) thanks to a strong collaboration of clinicians and researchers. Recent knowledge regarding the genetics of OI permits an accurate diagnosis of the specific type of OI and its own molecular mechanism, a genetic counseling for family planning and prenatal diagnosis, and in addition more targeted therapeutic options. A specific support with re-education for patients with OI is necessary and efficient. To optimize patient care, a multidisciplinary consultation is proposed at the CHUV, moreover a web site is available for patients, families and therapists: www.infomaladiesrares.ch

Consultation sur la dénonciation adressée à la Cour royale par M. le Cte de Montlosier

[Factum. Montlosier, François-Dominique de Reynaud (Comte de). 1826]

Consultation de MM. les bâtonniers de l'ordre des avocats du barreau de Paris en réponse aux questions posées par M. le Cte d'Haussonville...

[Haussonville (Joseph-Othenin-Bernard de Cléron, Cte d')]