Prevalence of papillary muscle hypertrophy in fabry disease

BACKGROUND AND AIMS: Fabry disease (FD) is an X-linked genetic lysosomal disease, in which a deficit in the alpha-galactosidase A enzyme results in lysosomal build-up of globotriaosylceramide in several organs, causing cardiac, renal and cerebrovascular complications. The aim of this study was to as...

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Detalles Bibliográficos
Autores principales: Cianciulli, Tomás Francisco, Saccheri, María Cristina, Llobera, Mariano Napoli, Balletti, Lorena Romina, Beck, Matín Alejandro, Morita, Luis Alberto, Lax, Jorge Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463397/
https://www.ncbi.nlm.nih.gov/pubmed/37635225
http://dx.doi.org/10.1186/s12872-023-03463-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463397/
https://www.ncbi.nlm.nih.gov/pubmed/37635225
http://dx.doi.org/10.1186/s12872-023-03463-w

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