TY - CHAP M1 - Book, Section TI - Desbuquois Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an autosomal recessive osteochondrodysplastic disease with typical skeletal anomalies and high mortality in the first year of life. It is part of a group of disease involved with multiple dislocations and characterized by severe prenatal and postnatal growth retardation (dwarfism < 5 SD), joint laxity, very short extremities, and progressive scoliosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164067820 ER -