TY  - JOUR
AU  - Hansford, Jordan R
AU  - Das, Anirban
AU  - McGee, Rose B
AU  - Nakano, Yoshiko
AU  - Brzezinski, Jack
AU  - Scollon, Sarah R
AU  - Rednam, Surya P
AU  - Schienda, Jaclyn
AU  - Michaeli, Orli
AU  - Kim, Sun Young
AU  - Greer, Mary-Louise C
AU  - Weksberg, Rosanna
AU  - Stewart, Douglas R
AU  - Foulkes, William D
AU  - Tabori, Uri
AU  - Pajtler, Kristian
AU  - Pfister, Stefan
AU  - Brodeur, Garrett M
AU  - Kamihara, Junne
TI  - Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors.
JO  - Clinical cancer research
VL  - 30
IS  - 11
SN  - 1078-0432
CY  - Philadelphia, Pa. [u.a.]
PB  - AACR
M1  - DKFZ-2024-00695
SP  - 2342-2350
PY  - 2024
N1  - 2024 Jun 3;30(11):2342-2350
AB  - Tumors of the central nervous system (CNS) comprise the second most common group of neoplasms in childhood. The incidence of germline predisposition among children with brain tumors continues to grow as our knowledge on disease aetiology increases. Some children with brain tumors may present with non-malignant phenotypic features of specific syndromes (e.g. nevoid basal cell carcinoma syndrome, neurofibromatosis type 1 and type 2, DICER1 syndrome, and constitutional mismatch repair deficiency), while others may present with a strong family history of cancer (e.g. Li-Fraumeni syndrome), or with a rare tumor commonly found in the context of germline predisposition (e.g. rhabdoid tumor predisposition syndrome). Approximately 50
LB  - PUB:(DE-HGF)16
C6  - pmid:38573059
DO  - DOI:10.1158/1078-0432.CCR-23-4033
UR  - https://inrepo02.dkfz.de/record/289300
ER  -