RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070142 T1 Jaffe Campanacci Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164070142 RD 2024/10/08 AB Syndrome of unknown etiology with variable expression characterized mainly by nonossifying fibromata, extraskeletal congenital anomalies such as café-au-lait spots, mental retardation, hypogonadism or cryptorchidism, and ocular and cardiovascular malformations. Other clinical features include chylothorax, stenosis of aortic isthmus, mitral insufficiency, chylopericardium, mental retardation, and precocious puberty.