Fabry Nephropathy: An Evidence-Based Narrative Review

Fabry Nephropathy: An Evidence-Based Narrative Review

Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enzyme α-galactosidase A. Complete or partial deficiency in this enzyme leads to intracellular accumulation of globotriaosylceramide (Gb3) and other glycosphingolipids in many cell types throughout the b...

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Bibliographic Details
Main Authors: María del Pino, Amado Andrés, Ana Ávila Bernabéu, Joaquín de Juan-Rivera, Elvira Fernández, Juan de Dios García Díaz, Domingo Hernández, José Luño, Isabel Martínez Fernández, José Paniagua, Manuel Posada de la Paz, José Carlos Rodríguez-Pérez, Rafael Santamaría, Roser Torra, Joan Torras Ambros, Pedro Vidau, Josep-Vicent Torregrosa
Format: Article
Language:English
Published: Karger Publishers 2018-03-01
Series:Kidney & Blood Pressure Research
Subjects:
Fabry disease
Nephropathy
Proteinuria
Enzyme replacement therapy
Inherited disorder
Online Access:https://www.karger.com/Article/FullText/488121

Internet

https://www.karger.com/Article/FullText/488121

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