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Updated: Jul 10, 2026

08:17
Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Severe visual impairment and retinal changes in a boy with a deletion of the gene for Nance-Horan syndrome
R Mathys1, H Deconinck, K Keymolen
1Department of Paediatric Ophthalmology, UZ Brussel, Brussels, Belgium. renske.mathys@uzbrussel.be
Bulletin De La Societe Belge D'Ophtalmologie
|November 21, 2007
Abstract:
We present the ophthalmologic findings in a boy with a deletion of Xp22 comprising the gene for Nance-Horan syndrome. Different mechanisms underlying the visual impairment in Nance-Horan syndrome are discussed.
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