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Erschienen in: Orphanet Journal of Rare Diseases 1/2010

Open Access 01.10.2010 | Poster presentation

DYSCERNE: developing clinical management guidelines for selected dysmorphic syndromes

verfasst von: Pam Griffiths, Kate Strong, Sara Gardner, Ruth Day, Caroline Harrison, Kerr Bronwyn, Kay Metcalfe, Han Brunner, Dian Donnai, Bruno Dallapiccola, Koenraad Devriendt, Malgorzata Krajewska-Walasek, Nicole Philip, Jill Clayton-Smith

Erschienen in: Orphanet Journal of Rare Diseases | Sonderheft 1/2010

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The DYSCERNE Network of Centres of Expertise for dysmorphology (http://​www.​dyscerne.​org), is developing clinical management guidelines for Williams (WS), Angelman (AS), Noonan (NS) and Kabuki (KS) syndromes. An initial scoping exercise identified these conditions as rare, complex, multi-system disorders, for which it was felt that affected patients, families and health/social care professionals would benefit from access to up-to-date evidence based management guidelines.
Published evidence from which to develop management recommendations for these conditions is very limited, and devising a systematic and robust methodology has been challenging. Our approach is based on the Scottish Intercollegiate Guidelines Network (SIGN) method, which we modified placing more emphasis on expert opinion and consensus, whilst maintaining systematic rigour and transparency of processes.
The development process includes:
- Identification of key management issues by guideline group leaders.
- Targeted, systematic literature searches using PubMed.
- Review, identification and grading of results by panel of invited experts.
- Consensus meetings at which experts present, discuss and agree recommendations.
- Initial drafting of guideline document which is circulated amongst experts and stakeholders for comments.
- Amendments incorporated and guidelines finalised.
- Guidelines piloted and evaluated.
- International dissemination.
The process has involved 49 experts from 8 countries reviewing between them, over 1000 papers. The WS guidelines are currently being piloted in 20 centres, by paediatricians and geneticists. The first draft of AS guidelines has been circulated for feedback. Consensus meetings for NS and KS will be held very shortly. The finished guidelines will be available from the DYSCERNE website.
Open AccessThis article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Titel
DYSCERNE: developing clinical management guidelines for selected dysmorphic syndromes
verfasst von
Pam Griffiths
Kate Strong
Sara Gardner
Ruth Day
Caroline Harrison
Kerr Bronwyn
Kay Metcalfe
Han Brunner
Dian Donnai
Bruno Dallapiccola
Koenraad Devriendt
Malgorzata Krajewska-Walasek
Nicole Philip
Jill Clayton-Smith
Publikationsdatum
01.10.2010
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe Sonderheft 1/2010
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-5-S1-P20

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