Neurofibromatosis type 1 guideline

 

 

ERN GENTURIS tumour surveillance guidelines for individuals with neurofibromatosis type 1

 

Authors: Charlotte Carton, D. Gareth Evans, Ignacio Blanco, Reinhard E. Friedrich, Rosalie E. Ferner, Said Farschtschi, Hector Salvador, Amedeo A. Azizi, Victor Mautner, Claas Röhl, Sirkku Peltonen, Stavros Stivaros, Eric Legius, and Rianne Oostenbrink,* On behalf of the ERN GENTURIS NF1 Tumour Management Guideline Group.

 

Full guideline document

Journal Publication1

Pocket guide2

Plain language summary3

Download the complete guidelines here.

Published online on 16 January 2023 in eClinicalMedicine: https://doi.org/10.1016/j.eclinm.2022.101818

The guide is available in the following languages (click on a flag to download the corresponding language version):  

                 

The plain language summary is available in the following languages (click on a flag to download the corresponding language version): 

1 The journal publication is a concise version of the full guideline document, published in a peer-reviewed journal.

2 The pocket guide is the guideline summary presented on a pocket card.

3 The plain language summary provides a clear summary of the guideline using non-technical language, making it accessible to a wider network of readers including patients.

 

Other relevant ERN GENTURIS information

ERN GENTURIS guideline development policy

ERN GENTURIS developed a policy regarding guideline development which is based on the principles of Grading of Recommendations Assessment, Development and Evaluation (GRADE) to ensure the quality of the guidelines, but is tailored for rare disease guidelines, using an “enhanced GRADE’ approach to mitigate the challenges associated with rare disease research (please see "Evidence evaluation in rare disease guidelines: a methodological perspective"). This approach includes a comprehensive literature search with expert opinion (from clinicians with expertise in the disease as well as patients), to ensure that guidelines are both evidence-based and clinically relevant to the complex needs of rare disease populations. More details can be found in our guideline development policy and terms of reference.

ERN GENTURIS website summary

Clinical practice guidelines  

ERN GENTURIS care pathway

ERN GENTURIS patient journey

ERN GENTURIS publications

ERN GENTURIS webinars

ERN GENTURIS brochure

Written by ERN GENTURIS

Endorsed by ERN GENTURIS*

Neurofibromatosis type 1 (NF1)

ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis)

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation.

Care pathway - Neurofibromatosis type 1

Patient journey - Neurofibromatosis type 1 (Translations **)

 

Patient journey – Counselling on reproductive options for individuals with a cancer predisposition syndrome (CPS) and relevant family members (Translations**)

Thematic Group 1: Schwannomatosis and neurofibromatosis

Neurofibromatosis type 1 (NF1)

 

ERN GENTURIS webinars

ERN GENTURIS webinars - Thematic group 1: Neurofibromatosis

Neurofibromatosis type 1 (NF1)

ERN GENTURIS brochure: Neurofibromatosis type 1 (NF1)

 

**Translations in multiple languages are available on our patient journey page.