Brief Clinical Report: Hypophosphatasia—Diagnostic Considerations and Treatment Outcomes in an Infant

Hypophosphatasia (HPP) is a rare, inherited metabolic bone disorder characterized by low serum alkaline phosphatase activity and impaired bone mineralization. Clinical manifestations and severity of symptoms vary widely in HPP, ranging from in utero death to isolated dental manifestations in adults....

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Detalles Bibliográficos
Autores principales: Duffus, Sara, Thrasher, Bradly, Calikoglu, Ali S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901473/
https://www.ncbi.nlm.nih.gov/pubmed/29808151
http://dx.doi.org/10.1155/2018/5719761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901473/
https://www.ncbi.nlm.nih.gov/pubmed/29808151
http://dx.doi.org/10.1155/2018/5719761

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