RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58088478 T1 Trisomy 4p 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=58088478 RD 2024/03/29 AB A rare chromosomal disorder in which all or a portion of the short arm (p) appears three times rather than twice in cells of the body. Clinically characterized by breathing difficulties, craniofacial anomalies, hands and feet abnormalities, and congenital heart defects. Other clinical features include genital anomalies in affected males, skeletal defects, and severe mental retardation.