REMINDER: Invitation to the next ERN-EYE webinar!

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This session is open to all!

Thursday 3rd February 2022,
6.30 pm - 7.30 pm CET

Neurofibromatosis 1 & 2: An Overview

ERN-EYE joint webinar with ERN Genturis, the ERN dedicated to Genetic Tumour Risk Syndromes.

Connection link will be sent shortly before the event. Registration is open until 3rd February, 12 am.

CLICK HERE TO REGISTER TO THE WEBINAR!

Webinar's programme

1) Overview of NF1 & NF2, recommendation, surveillance and new diagnostic criteria, Eric Legius, Leuven University Hospital, Belgium.

2) Ophthalmological aspects, retinal imaging & OCT of NF1 & NF2, and paediatric specificities of the care, Dominique Brémond-Gignac and Matthieu Robert, Hôpital Necker-Enfants Malades, Paris.

3) Molecular aspects of NF-1 and NF-2 and genetic testing, Kathleen Claes, Ghent University Hospital, Belgium.

4) Patient testimony, added value of the early genetic testing, Claas Röhl, Austrian center of expertise for Neurofibromatosis, Vienna, Austria.

Speakers

Pr Eric Legius
Center for Medical Genetics
Leuven University Hospital
Belgium

Pr Dominique Brémond-Gignac
Reference Center OPHTARA
Hôpital Necker-Enfants Malades, Paris, France

Pr Matthieu Robert
Reference Center OPHTARA
Hôpital Necker-Enfants Malades, Paris, France

Pr Kathleen Claes
Center for Medical Genetics
Ghent University Hospital, Belgium

Claas Röhl
Austrian center of expertise for Neurofibromatosis, Vienna, Austria
Member of the executive board of the ERN GENTURIS

More information about the speakers

See the replay of the past webinars

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