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Prosthetic rehabilitation of hypophosphatasia: a 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: Bağiş, Bora, Baltacioğlu, Esra, Aydoğan, Elif, Tamam, Evşen
Formato: Texto
Lenguaje:English
Publicado: Cases Network Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769366/
https://www.ncbi.nlm.nih.gov/pubmed/19918476
http://dx.doi.org/10.1186/1757-1626-2-7626

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