RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164087022
T1 Turcot 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=1164087022
RD 2024/04/18
AB A  polyposis  genetic  disorder  with  an  onset  in  adolescence  presenting  with  gastrointestinal  multiple  colorectal  adenomas  and  primary  central  nervous  system  (CNS)  tumors  (eg,  supratentorial  glioblastoma  and  cerebellar  medulloblastoma).  Other  clinical  features  include  café-au-lait  spots,  cutaneous  port-wine  stain,  and  focal  nodular  hyperplasia.