Sex Differences in Anderson–Fabry Cardiomyopathy: Clinical, Genetic, and Imaging Analysis in Women

Anderson–Fabry Disease (AFD) is a rare, systemic lysosomal storage disease triggered by mutations in the GLA gene, leading to α-galactosidase A (α-Gal A) deficiency. The disease’s X-linked inheritance leads to more severe, early-onset presentations in males, while females exhibit variable, often ins...

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Detalles Bibliográficos
Autores principales: Faro, Denise Cristiana, Losi, Valentina, Rodolico, Margherita Stefania, Torrisi, Elvira Mariateresa, Colomba, Paolo, Duro, Giovanni, Monte, Ines Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531426/
https://www.ncbi.nlm.nih.gov/pubmed/37761944
http://dx.doi.org/10.3390/genes14091804

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531426/
https://www.ncbi.nlm.nih.gov/pubmed/37761944
http://dx.doi.org/10.3390/genes14091804

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