Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/66740
Title: Ophthalmic manifestations in Mexican patients with Fabry disease [Manifestaciones oftalmológicas en pacientes mexicanos con enfermedad de Fabry]
Author: Beltran-Becerra, K.J.
Rios-Gonzalez, B.E.
Gutierrez-Amavizca, B.E.
Silva-Noriega, D.A.
Figuera, L.E.
Issue Date: 2012
Abstract: Fabry disease (FD) is a rare X-linked genetic lysosomal storage disease caused by a deficiency of the enzyme α-galactosidase A, that produces accumulation of globotriaosylceramide. There is a multisystemic involvement, including renal, cardiac, eye, and nervous system manifestations. Aim: To perform a descriptive analysis of the ophthalmological manifestations in Mexican patients with FD. Material and methods: We studied 13 patients with clinical and biochemical diagnostic of FD. Results: Cornea verticillata was found in 57% of men and 33% carriers. Conclusion: Cornea verticillata was the most common ocular manifestation in males and carriers of FD in Mexico. © 2011 Sociedad Española de Oftalmologa. Published by Elsevier España, S.L. All rights reserved.
URI: http://hdl.handle.net/20.500.12104/66740
Appears in Collections:Producción científica UdeG (prueba)

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