Review of Mechanisms, Pharmacological Management, Psychosocial Implications, and Holistic Treatment of Pain in Fabry Disease

Fabry disease is a progressive X-linked lysosomal storage disease caused by a mutation in the GLA gene, encoding the lysosomal hydrolase α-galactosidase A. The consequent reduced enzyme activity results in the toxic accumulation of glycosphingolipids, particularly globortriaosylceramide (Gb3 or GL(3...

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Detalles Bibliográficos
Autores principales: Rajan, Jonathan Niranjan, Ireland, Katharine, Johnson, Richard, Stepien, Karolina M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472766/
https://www.ncbi.nlm.nih.gov/pubmed/34575277
http://dx.doi.org/10.3390/jcm10184168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472766/
https://www.ncbi.nlm.nih.gov/pubmed/34575277
http://dx.doi.org/10.3390/jcm10184168

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