Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia

Hypophosphatasia (HPP) is a rare inherited metabolic disorder characterized by deficient activity of alkaline phosphatase, causing defective mineralization of bones and teeth. The symptoms vary from no symptoms to stillbirth or skeletal manifestations. Since 2015, asfotase alfa, an enzyme replacemen...

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Detalles Bibliográficos
Autores principales: Strandbech, Olivia Sarah, Lund, Allan, Ostergaard, Elsebet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100395/
https://www.ncbi.nlm.nih.gov/pubmed/33977024
http://dx.doi.org/10.1002/jmd2.12198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100395/
https://www.ncbi.nlm.nih.gov/pubmed/33977024
http://dx.doi.org/10.1002/jmd2.12198

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