TY - CHAP M1 - Book, Section TI - Maroteaux Cohen-Solal Bonaventure Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Severe congenital genetic disease characterized by undermineralization of skull and bones, thin ribs, thoracic collapse, multiple fractures, short stature, and prenatal onset. It is not believed to be linked to collagen metabolism defects. Facies is peculiar. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58075304 ER -