Download
s10689-021-00229-1.pdf 840,67KB
WeightNameValue
1000 Titel
  • Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group
1000 Autor/in
  1. Frühwald, Michael |
  2. Nemes, K. |
  3. Boztug, H. |
  4. Cornips, M. C. A. |
  5. Evans, Gareth |
  6. farah, roula |
  7. Glentis, Stavros |
  8. Jorgensen, M. |
  9. Katsibardi, Katerina |
  10. Hirsch, Steffen |
  11. Jahnukainen, K. |
  12. kventsel, iris |
  13. Kerl, Kornelius |
  14. Kratz, Christian |
  15. Pajtler, Kristian W. |
  16. Kordes, Uwe R. |
  17. Ridola, Vita |
  18. Stutz, E. |
  19. BOURDEAUT, Franck |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-02-03
1000 Erschienen in
1000 Quellenangabe
  • 20(4):305-316
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10689-021-00229-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484234/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The rhabdoid tumor (RT) predisposition syndromes 1 and 2 (RTPS1 and 2) are rare genetic conditions rendering young children vulnerable to an increased risk of RT, malignant neoplasms affecting the kidney, miscellaneous soft-part tissues, the liver and the central nervous system (Atypical Teratoid Rhabdoid Tumors, ATRT). Both, RTPS1&2 are due to pathogenic variants (PV) in genes encoding constituents of the BAF chromatin remodeling complex, i.e. SMARCB1 (RTPS1) and SMARCA4 (RTPS2). In contrast to other genetic disorders related to PVs in SMARCB1 and SMARCA4 such as Coffin-Siris Syndrome, RTPS1&2 are characterized by a predominance of truncating PVs, terminating transcription thus explaining a specific cancer risk. The penetrance of RTPS1 early in life is high and associated with a poor survival. However, few unaffected carriers may be encountered. Beyond RT, the tumor spectrum may be larger than initially suspected, and cancer surveillance offered to unaffected carriers (siblings or parents) and long-term survivors of RT is still a matter of discussion. RTPS2 exposes female carriers to an ill-defined risk of small cell carcinoma of the ovaries, hypercalcemic type (SCCOHT), which may appear in prepubertal females. RT surveillance protocols for these rare families have not been established. To address unresolved issues in the care of individuals with RTPS and to propose appropriate surveillance guidelines in childhood, the SIOPe Host Genome working group invited pediatric oncologists and geneticists to contribute to an expert meeting. The current manuscript summarizes conclusions of the panel discussion, including consented statements as well as non-evidence-based proposals for validation in the future.
1000 Sacherschließung
lokal Female [MeSH]
lokal Germline
lokal Brain Neoplasms/genetics [MeSH]
lokal Rhabdoid
lokal Transcription Factors/genetics [MeSH]
lokal Humans [MeSH]
lokal Rhabdoid Tumor/genetics [MeSH]
lokal Surveillance
lokal Rhabdoid Tumor/diagnosis [MeSH]
lokal Original Article
lokal Genetic Testing [MeSH]
lokal DNA Helicases/genetics [MeSH]
lokal Kidney Neoplasms/genetics [MeSH]
lokal SMARCB1 Protein/genetics [MeSH]
lokal ATRT
lokal Nuclear Proteins [MeSH]
lokal SMARCB1
lokal Central Nervous System Neoplasms [MeSH]
lokal Predisposition
lokal Child, Preschool [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-8237-1854|https://frl.publisso.de/adhoc/uri/TmVtZXMsIEsu|https://frl.publisso.de/adhoc/uri/Qm96dHVnLCBILg==|https://frl.publisso.de/adhoc/uri/Q29ybmlwcywgTS4gQy4gQS4=|https://orcid.org/0000-0002-8482-5784|https://orcid.org/0000-0002-6392-1590|https://orcid.org/0000-0002-9217-052X|https://frl.publisso.de/adhoc/uri/Sm9yZ2Vuc2VuLCBNLg==|https://orcid.org/0000-0001-8558-2561|https://orcid.org/0000-0002-4920-0930|https://frl.publisso.de/adhoc/uri/SmFobnVrYWluZW4sIEsu|https://orcid.org/0000-0003-4806-345X|https://orcid.org/0000-0002-5676-8102|https://orcid.org/0000-0003-4120-5873|https://orcid.org/0000-0002-3562-6121|https://orcid.org/0000-0001-6375-2320|https://orcid.org/0000-0001-8658-4702|https://frl.publisso.de/adhoc/uri/U3R1dHosIEUu|https://orcid.org/0000-0001-9489-6781
1000 Hinweis
  • DeepGreen-ID: 3154682389584adda0a5fdba448539b4 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Dateien
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6446067.rdf
1000 Erstellt am 2023-04-28T12:05:17.279+0200
1000 Erstellt von 322
1000 beschreibt frl:6446067
1000 Zuletzt bearbeitet Fri Oct 20 17:28:51 CEST 2023
1000 Objekt bearb. Fri Oct 20 17:28:51 CEST 2023
1000 Vgl. frl:6446067
1000 Oai Id
  1. oai:frl.publisso.de:frl:6446067 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

View source