Paediatric syndromes with cancer predisposition

There are many genetic syndromes that are associated with an increased risk of cancer. These syndromes are rare, and can involve multiple systems. Often there is a lack of data to inform the development of evidence based management advice. It is usually beyond the scope of the eviQ paediatric cancer genetics reference committee to develop management protocols for this group of rare disorders. To assist eviQ users, members of the eviQ paediatric cancer genetics reference committee have contributed to a list of resources for some of these rare syndromes. Users should note that this list is incomplete and inclusion in the list does not indicate endorsement of the resource as accurate. Clinical judgement should be used when accessing information from these resources. If a clinician is aware of a reliable and useful resource they would like to be considered for inclusion in the table please email feedback@eviq.org.au

See  Paediatric syndromes with cancer predisposition

Version 3

Date	Summary of changes
14/10/2022	Table changed from Excel file to PDF. Other minor formatting changes throughout document. Version number increased to V.3.

Version 2

Date	Summary of changes
06/06/2022	Juvenile polyposis of infancy (10q23 deletion) added to the table. Version increased to V.2. To be reviewed at next scheduled review date.

Version 1

Date	Summary of changes
22/02/2022	New document developed and discussed at July 2021 paediatric cancer genetics reference committee meeting. Discussions continued by email and MS Teams.Approved for publication as V.1. Review in 1 year.