RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58088534 T1 Trisomy 9 T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58088534 RD 2024/10/10 AB Chromosomal disorder that can occur in a mosaic or nonmosaic expression, in which all major systems are significantly involved. Clinically characterized by severe gastrointestinal problems, scoliosis and kyphosis, repetitive periods of apnea, complex congenital heart defects, severe immunological disorders, failure to thrive, and severe mental retardation. Death occurs in infancy or early childhood.