RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164087842 T1 Watson Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164087842 RD 2024/03/28 AB A rare disease combining moderate to severe pulmonary valvular stenosis with “café-au-lait” spots, macrocephaly, decreased intelligence, neurofibromas, and short stature. Other features include macrocephaly and Lisch nodules. Neurofibromas are usually present in 30% of affected individuals. In most cases, it is a condition that overlaps those of neurofibromatosis and Noonan Syndrome.