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Description

Après sa formation à l'Université libre de Bruxelles et son diplôme Européen d'ophtalmologie obtenu en 2008, le Docteur Depasse a choisi de se spécialiser en ophtalmologie pédiatrique ainsi qu'en ophtalmologie génétique. Elle a complété sa formation en strabologie à l'Université de Nantes et a exercée ces spécialités pendant près de 10 ans à l'hôpital Erasme, à l'hôpital des Enfants Reine Fabiola, à l'hôpital Brugmann et jusque fin 2019 au CHU de Charleroi, dont elle a dirigé le service d'ophtalmologie. Elle exerce aujourd'hui sa spécialité au sein du Cabinet Ophtalmo BXL et à l'HUDERF. Depuis 2013, elle est également reconnue comme médecin revalidateur en basse vision. Elle est actuellement médecin directeur du Centre de Revalidation Fonctionnelle des Amis des Aveugles.

Specialties - Fanny Depasse

  • Ophtalmo-pédiatrie
  • Ophtalmo-génétique
  • Basse vision

Expertises

Pediatric

Map

CV

STUDIES

  • docteur en médecine 2004
  • ophtalmologie 2008
  • revalidateur 2013

PROFESSIONAL EXPERIENCE

  • Hôpital Erasme
  • HUDERF
  • Centre HORUS
  • Hôpital Marie Curie

Organisations member

  • SFO, Pedlow, ARIBA, SBO

Participation in conferences

  • Participation à des congrès et conférences, en tant qu'orateur et que participant, en Belgique (SBO, OB, symposium, ...)et en France (SFO, colloque starbologie, ARIBA, ...)

Spoken languages

  • Français
  • Nederlands

Academic Research and Publications

  • Coppieters F, Van Schil K, Bauwens M, Verdin H, De Jaegher A, Syx D, Sante T, Lefever S, Abdelmoula NB, Depasse F, Casteels I, de Ravel T, Meire F, Leroy BP, De Baere E., « Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. », Genet Med. 2014 Sep;16(9):671-80. doi: 10.1038/gim.2014.24. Epub 2014 Mar 13.
  • Roulez FM, Faes F, Delbeke P, Van Bogaert P, Rodesch G, De Zaeytijd J, Depasse F, Coucke PJ, Meire FM., « Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome. », J Neuroophthalmol. 2014 Jun;34(2):137-43.
  • Van Schil K, Karlstetter M, Aslanidis A, Dannhausen K, Azam M, Qamar R, Leroy BP, Depasse F, Langmann T, De Baere E. Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7. Sci Rep. 2016 Feb 18;6:21307.
  • Van Cauwenbergh C, Coppieters F, Roels D, De Jaegere S, Flipts H, De Zaeytijd J, Walraedt S, Claes C, Fransen E, Van Camp G, Depasse F, Casteels I, de Ravel T, Leroy BP, De Baere E. Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. PLoS One. 2017 Jan 11;12(1):e0170038
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