Ripperger, Tim ORCID: 0000-0001-6470-8612, Bielack, Stefan S., Borkhardt, Arndt, Brecht, Ines B., Burkhardt, Birgit, Calaminus, Gabriele, Debatin, Klaus-Michael ORCID: 0000-0002-8397-1886, Deubzer, Hedwig, Dirksen, Uta, Eckert, Cornelia, Eggert, Angelika, Erlacher, Miriam, Fleischhack, Gudrun, Fruehwald, Michael C., Gnekow, Astrid, Goehring, Gudrun, Graf, Norbert ORCID: 0000-0002-2248-323X, Hanenberg, Helmut, Hauer, Julia, Hero, Barbara, Hettmer, Simone, von Hoff, Katja, Horstmann, Martin, Hoyer, Juliane, Illig, Thomas, Kaatsch, Peter, Kappler, Roland ORCID: 0000-0002-8581-2803, Kerl, Kornelius, Klingebiel, Thomas, Kontny, Udo, Kordes, Uwe ORCID: 0000-0001-6375-2320, Koerholz, Dieter, Koscielniak, Ewa, Kramm, Christof M., Kuhlen, Michaela, Kulozik, Andreas E., Lamottke, Britta, Leuschner, Ivo, Lohmann, Dietmar R. ORCID: 0000-0002-2624-9889, Meinhardt, Andrea, Metzler, Markus ORCID: 0000-0002-4523-1676, Meyer, Lder H., Moser, Olga, Nathrath, Michaela, Niemeyer, Charlotte M., Nustede, Rainer, Pajtler, Kristian W. ORCID: 0000-0002-3562-6121, Paret, Claudia ORCID: 0000-0002-9094-1634, 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 ORCID: 0000-0002-3834-0727, Steinemann, Doris, Strahm, Brigitte, Temming, Petra, Thomay, Kathrin, von Bueren, Andre O., Vorwerk, Peter, Witt, Olaf, Wlodarski, Marcin, Woessmann, Willy, Zenker, Martin, Zimmermann, Stefanie, Pfister, Stefan M. and Kratz, Christian P. (2017). Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology. Am. J. Med. Genet. A, 173 (4). S. 1017 - 1038. HOBOKEN: WILEY. ISSN 1552-4833

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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.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Ripperger, TimUNSPECIFIEDorcid.org/0000-0001-6470-8612UNSPECIFIED
Bielack, Stefan S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Borkhardt, ArndtUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Brecht, Ines B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Burkhardt, BirgitUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Calaminus, GabrieleUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Debatin, Klaus-MichaelUNSPECIFIEDorcid.org/0000-0002-8397-1886UNSPECIFIED
Deubzer, HedwigUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Dirksen, UtaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Eckert, CorneliaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Eggert, AngelikaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Erlacher, MiriamUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fleischhack, GudrunUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fruehwald, Michael C.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gnekow, AstridUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Goehring, GudrunUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Graf, NorbertUNSPECIFIEDorcid.org/0000-0002-2248-323XUNSPECIFIED
Hanenberg, HelmutUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hauer, JuliaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hero, BarbaraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hettmer, SimoneUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
von Hoff, KatjaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Horstmann, MartinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hoyer, JulianeUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Illig, ThomasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kaatsch, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kappler, RolandUNSPECIFIEDorcid.org/0000-0002-8581-2803UNSPECIFIED
Kerl, KorneliusUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Klingebiel, ThomasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kontny, UdoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kordes, UweUNSPECIFIEDorcid.org/0000-0001-6375-2320UNSPECIFIED
Koerholz, DieterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Koscielniak, EwaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kramm, Christof M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kuhlen, MichaelaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kulozik, Andreas E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lamottke, BrittaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Leuschner, IvoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lohmann, Dietmar R.UNSPECIFIEDorcid.org/0000-0002-2624-9889UNSPECIFIED
Meinhardt, AndreaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Metzler, MarkusUNSPECIFIEDorcid.org/0000-0002-4523-1676UNSPECIFIED
Meyer, Lder H.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Moser, OlgaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nathrath, MichaelaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Niemeyer, Charlotte M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nustede, RainerUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pajtler, Kristian W.UNSPECIFIEDorcid.org/0000-0002-3562-6121UNSPECIFIED
Paret, ClaudiaUNSPECIFIEDorcid.org/0000-0002-9094-1634UNSPECIFIED
Rasche, MareikeUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Reinhardt, DirkUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Riess, OlafUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Russo, AlexandraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Rutkowski, StefanUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schlegelberger, BrigitteUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schneider, DominikUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schneppenheim, ReinhardUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schrappe, MartinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schroeder, ChristopherUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
von Schweinitz, DietrichUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Simon, ThorstenUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Sparber-Sauer, MonikaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Spix, ClaudiaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Stanulla, MartinUNSPECIFIEDorcid.org/0000-0002-3834-0727UNSPECIFIED
Steinemann, DorisUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Strahm, BrigitteUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Temming, PetraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Thomay, KathrinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
von Bueren, Andre O.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Vorwerk, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Witt, OlafUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wlodarski, MarcinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Woessmann, WillyUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zenker, MartinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zimmermann, StefanieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pfister, Stefan M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kratz, Christian P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-235801
DOI: 10.1002/ajmg.a.38142
Journal or Publication Title: Am. J. Med. Genet. A
Volume: 173
Number: 4
Page Range: S. 1017 - 1038
Date: 2017
Publisher: WILEY
Place of Publication: HOBOKEN
ISSN: 1552-4833
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; LI-FRAUMENI SYNDROME; FAMILIAL ADENOMATOUS POLYPOSIS; TUMOR-SUPPRESSOR GENE; BIALLELIC FANCD1/BRCA2 MUTATIONS; JUVENILE MYELOMONOCYTIC LEUKEMIA; GASTROINTESTINAL STROMAL TUMORS; TUBEROUS SCLEROSIS COMPLEX; ACUTE MYELOGENOUS LEUKEMIAMultiple languages
Genetics & HeredityMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/23580

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