TY - CHAP M1 - Book, Section TI - Maroteaux Cohen-Solal Bonaventure Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Severe congenital genetic disease characterized by undermineralization of skull and bones, thin ribs, thoracic collapse, multiple fractures, short stature, and prenatal onset. Normal facies accompany this disorder. Clinically, the patient present numerous pathological bone fractures like those affected with the lethal form of osteogenesis imperfecta, but the former can be differentiated by a thin-bone group of lethal dysplasias. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164077819 ER -