Hypophosphatasia: Current Literature for Pathophysiology, Clinical Manifestations, Diagnosis, and Treatment

Hypophosphatasia (HPP) is a rare inherited bone disorder identified by impaired bone mineralization. There are seven subtypes of HPP mainly characterized by their age of onset. These subtypes consist of perinatal (prenatal) benign, perinatal lethal, infantile, childhood, adult, odontohypophosphatasi...

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Detalles Bibliográficos
Autores principales: Bangura, Abdulai, Wright, Lisa, Shuler, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362651/
https://www.ncbi.nlm.nih.gov/pubmed/32676235
http://dx.doi.org/10.7759/cureus.8594

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362651/
https://www.ncbi.nlm.nih.gov/pubmed/32676235
http://dx.doi.org/10.7759/cureus.8594

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