Future directions in managing aniridia-associated keratopathy

Congenital aniridia is a panocular disorder that is typically characterized by iris hypoplasia and aniridia-associated keratopathy (AAK). AAK results in the progressive loss of corneal transparency and thereby loss of vision. Currently, there is no approved therapy to delay or prevent its progressio...

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Veröffentlicht in:Survey of ophthalmology 2023-09, Vol.68 (5), p.940-956
Hauptverfasser: van Velthoven, Arianne J.H., Utheim, Tor P., Notara, Maria, Bremond-Gignac, Dominique, Figueiredo, Francisco C., Skottman, Heli, Aberdam, Daniel, Daniels, Julie T., Ferrari, Giulio, Grupcheva, Christina, Koppen, Carina, Parekh, Mohit, Ritter, Thomas, Romano, Vito, Ferrari, Stefano, Cursiefen, Claus, Lagali, Neil, LaPointe, Vanessa L.S., Dickman, Mor M.
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Sprache:eng
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Zusammenfassung:Congenital aniridia is a panocular disorder that is typically characterized by iris hypoplasia and aniridia-associated keratopathy (AAK). AAK results in the progressive loss of corneal transparency and thereby loss of vision. Currently, there is no approved therapy to delay or prevent its progression, and clinical management is challenging because of phenotypic variability and high risk of complications after interventions; however, new insights into the molecular pathogenesis of AAK may help improve its management. Here, we review the current understanding about the pathogenesis and management of AAK. We highlight the biological mechanisms involved in AAK development with the aim to develop future treatment options, including surgical, pharmacological, cell therapies, and gene therapies.
ISSN:0039-6257
1879-3304
1879-3304
DOI:10.1016/j.survophthal.2023.04.003