Hyperphosphatemic Familial Tumoral Calcinosis With Galnt3 Mutation: Transient Response to Anti‐Interleukin‐1 Treatments

Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare autosomal recessive disease caused by mutations in genes involved in phosphate homeostasis and characterized by high serum phosphate concentration and occurrence of ectopic calcifications. Management of the disease includes lowering of p...

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Detalles Bibliográficos
Autores principales: Dauchez, Astrid, Souffir, Camille, Quartier, Pierre, Baujat, Geneviève, Briot, Karine, Roux, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659445/
https://www.ncbi.nlm.nih.gov/pubmed/31372591
http://dx.doi.org/10.1002/jbm4.10185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659445/
https://www.ncbi.nlm.nih.gov/pubmed/31372591
http://dx.doi.org/10.1002/jbm4.10185

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