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 accesspediatrics.mhmedical.com/content.aspx?aid=1164070142
RD 2024/04/23
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.