Please use this identifier to cite or link to this item: doi:10.22028/D291-41051
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Title: Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Author(s): Ripperger, Tim
Bielack, Stefan S.
Borkhardt, Arndt
Brecht, Ines B.
Burkhardt, Birgit
Calaminus, Gabriele
Debatin, Klaus-Michael
Deubzer, Hedwig
Dirksen, Uta
Eckert, Cornelia
Eggert, Angelika
Erlacher, Miriam
Fleischhack, Gudrun
Frühwald, Michael C.
Gnekow, Astrid
Goehring, Gudrun
Graf, Norbert
Hanenberg, Helmut
Hauer, Julia
Hero, Barbara
Hettmer, Simone
von Hoff, Katja
Horstmann, Martin
Hoyer, Juliane
Illig, Thomas
Kaatsch, Peter
Kappler, Roland
Kerl, Kornelius
Klingebiel, Thomas
Kontny, Udo
Kordes, Uwe
Körholz, Dieter
Koscielniak, Ewa
Kramm, Christof M.
Kuhlen, Michaela
Kulozik, Andreas E.
Lamottke, Britta
Leuschner, Ivo
Lohmann, Dietmar R.
Meinhardt, Andrea
Metzler, Markus
Meyer, Lüder H.
Moser, Olga
Nathrath, Michaela
Niemeyer, Charlotte M.
Nustede, Rainer
Pajtler, Kristian W.
Paret, Claudia
Rasche, Mareike
Reinhardt, Dirk
Rieß, Olaf
Russo, Alexandra
Rutkowski, Stefan
Schlegelberger, Brigitte
Schneider, Dominik
Schneppenheim, Reinhard
Schrappe, Martin
Schroeder, Christopher
von Schweinitz, Dietrich
Simon, Thorsten
Sparber-Sauer, Monika
Spix, Claudia
Stanulla, Martin
Steinemann, Doris
Strahm, Brigitte
Temming, Petra
Thomay, Kathrin
von Bueren, Andre O.
Vorwerk, Peter
Witt, Olaf
Wlodarski, Marcin
Wössmann, Willy
Zenker, Martin
Zimmermann, Stefanie
Pfister, Stefan M.
Kratz, Christian P.
Language: English
Title: American Journal of Medical Genetics. Part A
Volume: 173
Issue: 4
Pages: 1017-1037
Publisher/Platform: Wiley
Year of Publication: 2017
Free key words: genetic cancer predisposition
genetic predisposition testing
genetic screening
germline mutation
hereditary cancer syndrome
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: Heritable predisposition is an important cause of cancer in children and adolescents. Although a large number of cancer predisposition genes and their associated syndromes and malignancies have already been described, it appears likely that there are more pediatric cancer patients in whom heritable cancer predisposition syndromes have yet to be recognized. In a consensus meeting in the beginning of 2016, we convened experts in Human Genetics and Pediatric Hematology/Oncology to review the available data, to categorize the large amount of information, and to develop recommendations regarding when a cancer predisposition syndrome should be suspected in a young oncology patient. This review summarizes the current knowledge of cancer predisposition syndromes in pediatric oncology and provides essential information on clinical situations in which a childhood cancer predisposition syndrome should be suspected.
DOI of the first publication: 10.1002/ajmg.a.38142
URL of the first publication: https://doi.org/10.1002/ajmg.a.38142
Link to this record: urn:nbn:de:bsz:291--ds-410518
hdl:20.500.11880/36842
http://dx.doi.org/10.22028/D291-41051
ISSN: 1552-4833
1552-4825
Date of registration: 13-Nov-2023
Description of the related object: Supporting Information
Related object: https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fajmg.a.38142&file=ajmga38142-sup-0001-SuppInfo-S1.docx
Faculty: M - Medizinische Fakultät
Department: M - Pädiatrie
Professorship: M - Prof. Dr. Norbert Graf
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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