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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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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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author Bağiş, Bora
Baltacioğlu, Esra
Aydoğan, Elif
Tamam, Evşen
author_facet Bağiş, Bora
Baltacioğlu, Esra
Aydoğan, Elif
Tamam, Evşen
author_sort Bağiş, Bora
collection PubMed
description 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 disease are respiratory complications, premature craniosynostosis, widespread demineralization and rachitic changes in the metaphases, stress fractures, chondrocalcinosis and osteoarthropathy. Characteristic dental symptoms are premature deciduous teeth loss, premature exfoliation of fully rooted primary teeth, severe dental caries and alveolar bone loss. This clinical report describes the prosthetic rehabilitation of a twenty two year-old Turkish female patient with hypophosphatasia.
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spelling pubmed-27693662009-11-16 Prosthetic rehabilitation of hypophosphatasia: a case report Bağiş, Bora Baltacioğlu, Esra Aydoğan, Elif Tamam, Evşen Cases J 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 disease are respiratory complications, premature craniosynostosis, widespread demineralization and rachitic changes in the metaphases, stress fractures, chondrocalcinosis and osteoarthropathy. Characteristic dental symptoms are premature deciduous teeth loss, premature exfoliation of fully rooted primary teeth, severe dental caries and alveolar bone loss. This clinical report describes the prosthetic rehabilitation of a twenty two year-old Turkish female patient with hypophosphatasia. Cases Network Ltd 2008-12-12 /pmc/articles/PMC2769366/ /pubmed/19918476 http://dx.doi.org/10.1186/1757-1626-2-7626 Text en © 2009 Bağiş et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Bağiş, Bora
Baltacioğlu, Esra
Aydoğan, Elif
Tamam, Evşen
Prosthetic rehabilitation of hypophosphatasia: a case report
title Prosthetic rehabilitation of hypophosphatasia: a case report
title_full Prosthetic rehabilitation of hypophosphatasia: a case report
title_fullStr Prosthetic rehabilitation of hypophosphatasia: a case report
title_full_unstemmed Prosthetic rehabilitation of hypophosphatasia: a case report
title_short Prosthetic rehabilitation of hypophosphatasia: a case report
title_sort prosthetic rehabilitation of hypophosphatasia: a case report
topic Case report
url 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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