RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164081576
T1 Peutz-Jeghers 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=1164081576
RD 2024/04/25
AB A  genetic  disorder  leading  to  congenital  hamartomatous  polyps  of  the  gastrointestinal  tract  associated  with  perioral  melanin  spots.  There  is  an  increased  risk  of  malignancy.