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After her training at the Free University of Brussels and her European diploma in ophthalmology obtained in 2008, Dr. Depasse chose to specialize in pediatric ophthalmology as well as in genetic ophthalmology. She completed her training in strabology at the University of Nantes and practiced these specialties for nearly 10 years at the Erasme Hospital, the Queen Fabiola Children's Hospital, the Brugmann Hospital and until the end of 2019 at the University Hospital of Charleroi, where she headed the ophthalmology department. Today she practices her specialty at the Cabinet Ophtalmo BXL and at the HUDERF. Since 2013, she is also recognized as a revalidating doctor in low vision. She is currently the managing doctor of the Functional Revalidation Center of Friends of the Blind.

The description was edited by the doctoranytime team, based on verified information.

Specialization and Experience

  • Pediatric

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  • Doctor of Medicine 2004+Ophthalmology 2008+Revalidator 2013
  • ophtalmologie 2008
  • revalidateur 2013

Professional experience

  • Erasmus Hospital+HUDERF+HORUS Center+Marie Curie Hospital
  • 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

  • French
  • Dutch

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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Dr. Fanny Depasse is situated at Rue Roosendael 225 bte 7 in Forest.

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