Objective: Retrospective analysis of the famous painter Edgar Degas' eye disease.
Design: A historical review and analysis based on Degas' paintings and letters exchanged between the painter and his friends and family members, as well as on the chronicles of his associates. DeGas-Musson family papers at the Howard-Tilton Library of Tulane University are also reviewed.
Results: Degas had an eye disease that was first noticed in 1870 and that progressed throughout his life. He suffered from progressive bilateral central visual loss and light sensitivity which was most acutely recognized while he was visiting his mother's side of the family in New Orleans where he could not paint outside because of the bright sun. Edgar's maternal first cousin, Estelle Musson, also suffered gradual bilateral visual loss, and was also known to have light sensitivity early in her life. Estelle became totally blind in her early 30s. Both Edgar and Estelle were otherwise healthy and lived long lives.
Conclusion: It is likely that Edgar Degas and his cousin Estelle Musson had a hereditary retinal degeneration primarily affecting their central vision. Degas' retinal disease undoubtedly affected his life and his art but did not prevent him from being one of the most admired painters of all times.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1080/13816810701351313 | DOI Listing |
Ophthalmic Genet
August 2021
Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, Palo Alto, California, USA.
Renowned French painter Edgar Degas suffered of progressive light sensitivity and blurred central vision in both eyes, which affected his life and art in many ways. A first cousin from his mother's side, Estelle Musson of New Orleans also lost vision in a similar fashion at a comparable age. We postulated that Edgar and Estelle shared the same retinal pathology that possibly developed in a hereditary fashion, and we were interested whether any of their living family descendants might carry mutations to test the possibility that Edgar Degas may have had Stargardt disease.
View Article and Find Full Text PDFArch Soc Esp Oftalmol (Engl Ed)
February 2019
Servicio de Oftalmología, Hospital La Paz, Madrid, España. Electronic address:
Sci Rep
August 2016
Australian Synchrotron, Clayton, Victoria, Australia.
The preservation and understanding of cultural heritage depends increasingly on in-depth chemical studies. Rapid technological advances are forging connections between scientists and arts communities, enabling revolutionary new techniques for non-invasive technical study of culturally significant, highly prized artworks. We have applied a non-invasive, rapid, high definition X-ray fluorescence (XRF) elemental mapping technique to a French Impressionist painting using a synchrotron radiation source, and show how this technology can advance scholarly art interpretation and preservation.
View Article and Find Full Text PDFArch Soc Esp Oftalmol
June 2017
Servicio de Oftalmología, Hospital La Paz, Madrid, España. Electronic address:
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!