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Prosthetic rehabilitation of a young patient with Hypophosphatasia – A review and case report

Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene. Six clinical forms of hypophosphatasia are recognized. Systemic symptoms of the...

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Detalles Bibliográficos
Autores principales: Grewal, Partapjot S., Gupta, Kanu Priya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341764/
https://www.ncbi.nlm.nih.gov/pubmed/22557902
http://dx.doi.org/10.4103/0976-237X.94551