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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Bağiş, Bora, Baltacioğlu, Esra, Aydoğan, Elif, Tamam, Evşen
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cases Network Ltd 2008
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2769366/
https://ncbi.nlm.nih.gov/pubmed/19918476
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-2-7626
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