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Dental effects of enzyme replacement therapy in case of childhood-type hypophosphatasia
BACKGROUND: Hypophosphatasia (HPP), a skeletal disease characterized by hypomineralization of bone and teeth, is caused by an ALPL gene mutation that leads to low activity of the tissue non-specific alkaline phosphatase enzyme. Although enzyme replacement therapy (ERT) was recently introduced for af...
Autores principales: | Okawa, Rena, Kokomoto, Kazuma, Nakano, Kazuhiko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237502/ https://www.ncbi.nlm.nih.gov/pubmed/34176466 http://dx.doi.org/10.1186/s12903-021-01673-2 |
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