Screening for Fabry’s disease in a high-risk subpopulation of FMF

BACKGROUND: Familial Mediterranean fever (FMF) is an autosomal recessive disease associated with mutations in the Mediterranean fever gene (MEFV) that manifests with recurrent episodes of febrile serositis. Fabry’s disease (FD) is an X-linked lysosomal storage disease caused by mutations in the alph...

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Detalles Bibliográficos
Autores principales: Maller, Tomer, Ben-Zvi, Ilan, Lidar, Merav, Livneh, Avi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585770/
https://www.ncbi.nlm.nih.gov/pubmed/36271470
http://dx.doi.org/10.1186/s40001-022-00846-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585770/
https://www.ncbi.nlm.nih.gov/pubmed/36271470
http://dx.doi.org/10.1186/s40001-022-00846-1

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