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doi:10.22028/D291-41051
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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