Burden of disease in pediatric patients with hypophosphatasia: results from the HPP Impact Patient Survey and the HPP Outcomes Study Telephone interview

BACKGROUND: Hypophosphatasia (HPP) is a rare, inherited, metabolic bone disease caused by deficient tissue-non-specific isoenzyme of alkaline phosphatase activity that manifests as a broad range of signs/symptoms, including bone mineralization defects and systemic complications. The burden of diseas...

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Detalles Bibliográficos
Autores principales: Rush, Eric T., Moseley, Scott, Petryk, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698035/
https://www.ncbi.nlm.nih.gov/pubmed/31419999
http://dx.doi.org/10.1186/s13023-019-1167-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698035/
https://www.ncbi.nlm.nih.gov/pubmed/31419999
http://dx.doi.org/10.1186/s13023-019-1167-5

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