Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphatasia: a systematic literature review

BACKGROUND: Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by tissue-nonspecific alkaline phosphatase deficiency, characterized by bone mineralization defects and systemic complications. Understanding of the clinical course and burden of HPP is limited by its rarity. This syst...

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Detalles Bibliográficos
Autores principales: Szabo, Shelagh M., Tomazos, Ioannis C., Petryk, Anna, Powell, Lauren C., Donato, Bonnie M. K., Zarate, Yuri A., Tiulpakov, Anatoly, Martos-Moreno, Gabriel Ángel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485115/
https://www.ncbi.nlm.nih.gov/pubmed/31023354
http://dx.doi.org/10.1186/s13023-019-1062-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485115/
https://www.ncbi.nlm.nih.gov/pubmed/31023354
http://dx.doi.org/10.1186/s13023-019-1062-0

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