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Long-term outcome of cultured corneal endothelial cell transplantation with descemetorhexis: A 10-year follow-up study. [PDF]

Am J Ophthalmol Case Rep
Kataoka Y, Tomioka Y, Ueno M, Kitazawa K, Fukuoka H, Okumura N, Koizumi N, Sotozono C, Kinoshita S.   +8 more
europepmc   +1 more source

The Genetic Basis of Fuchs Endothelial Corneal Dystrophy

Journal of Ophthalmic & Vision Research, 2010
Sepehr Feizi
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Fuchs' endothelial dystrophy of the cornea

Survey of Ophthalmology, 1993
Fuchs' endothelial dystrophy of the cornea is a significant cause of corneal blindness in the United States. The disease is characterized by a slow, continuous loss of morphologically and physiologically altered endothelial cells, eventually leading to corneal edema.
A P, Adamis, V, Filatov, B J, Tripathi, R C, Tripathi   +3 more
openaire   +4 more sources

Fuchs endothelial corneal dystrophy

Vestnik oftal'mologii, 2017
Fuchs endothelial dystrophy is a severe disease characterized by slowly progressing bilateral asymmetric corneal edema usually seen in elderly patients. The primary purpose of treatment is to minimize edema-related symptoms, such as ocular discomfort and visual acuity loss.
S V, Trufanov, E P, Salovarova, S A, Malozhen, R Z, Bagh   +3 more
openaire   +2 more sources

Fuchs’ endothelial dystrophy

Optician, 2022
Optometrist Kirit Patel discusses a case concerning a patient with a common corneal condition that we all encounter in general practice and illustrates how it can be managed without the need for referral
openaire   +1 more source

Inheritance of Fuchs' Endothelial Dystrophy

Archives of Ophthalmology, 1971
Two pedigrees contain seven individuals with documented Fuchs' endothelial dystrophy. A review of all previously reported familial cases reveals one pedigree with sufficient useful data for genetic analysis. Study of these three pedigrees together with segregation analysis suggests an autosomal dominant mutation as the most likely etiology, although ...
H E, Cross, A E, Maumenee, S J, Cantolino   +2 more
openaire   +2 more sources

Mechanisms of disease: Fuchs' endothelial dystrophy

Ophthalmology Clinics of North America, 2002
Fuchs' endothelial dystrophy is a common disease that has been widely studied since its initial report in 1910 by Ernst Fuchs. Although its clinical course and pathologic characteristics are well described, the etiology and inheritance pattern are still ambiguous.
Sheila, Borboli, Kathryn, Colby
openaire   +2 more sources

Oxytalan Fibers in Fuchs' Endothelial Dystrophy

Archives of Ophthalmology, 1981
• In a histochemical and electron microscopic study of nine cases of Fuchs' endothelial dystrophy, oxytalan, a component of the elastic fiber family, was found in the extracellular tissues of the cornea. Oxytalan was most abundant around but not within the guttate excrescences; it was also found beneath the epithelium, occasionally beneath Bowman's ...
R A, Alexander, I, Grierson, A, Garner
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Endothelial viral inclusions in Fuchs' corneal dystrophy

Human Pathology, 1987
A case of Fuchs' corneal dystrophy is presented. The patient, a 70-year-old white woman, had bilateral decreasing vision, especially while reading and driving at night. Clinical features were characteristic of Fuchs' corneal dystrophy. Ultrastructural studies demonstrated findings in Descemet's membrane typical of those previously reported with ...
S I, Roth, E L, Stock, R, Jutabha
openaire   +2 more sources